Variant Name |
Variant Type |
Location in Gene |
Related Gene |
No. of Studies (Positive/Negative/Trend)  |
Overlap with SZ |
Overlap with MDD |
5HTTLPR |
microsatellite |
promoter |
SLC6A4
|
41 (12/29/0) |
YES
|
YES
|
BDNF Val66Met |
point mutation |
|
BDNF
|
21 (11/10/0) |
YES
|
YES
|
SLC6A4 intron2 VNTR |
VNTR |
intron2 |
SLC6A4
|
16 (4/12/0) |
YES
|
YES
|
COMT Val158Met |
point mutation |
|
COMT
|
14 (2/12/0) |
NO
|
YES
|
MTHFR C677T |
point mutation |
|
MTHFR
|
13 (5/8/0) |
YES
|
YES
|
MAOA promoter VNTR |
VNTR |
promoter |
MAOA
|
9 (0/9/0) |
NO
|
YES
|
DRD3 Ser9Gly |
point mutation |
|
DRD3
|
9 (2/7/0) |
NO
|
YES
|
HTR2A C102T |
point mutation |
|
HTR2A
|
8 (0/8/0) |
YES
|
YES
|
MAOA (CA)n |
microsatellite |
|
MAOA
|
8 (5/3/0) |
NO
|
YES
|
DRD4 exon3 VNTR |
VNTR |
exon3 |
DRD4
|
8 (1/7/0) |
YES
|
YES
|
TPH1 A218C |
point mutation |
intron 7 |
TPH1
|
6 (2/4/0) |
YES
|
YES
|
DRD3 BalI Polymorphism |
point mutation |
|
DRD3
|
6 (1/5/0) |
NO
|
NO
|
5-HTT intron 2 VNTR |
VNTR |
|
SLC6A4
|
5 (1/4/0) |
NO
|
YES
|
TH intron 1 tetranucleotide repeat |
duplication |
intron 1 |
TH
|
5 (0/5/0) |
NO
|
YES
|
DRD1 -48A/G |
point mutation |
|
DRD1
|
5 (3/2/0) |
YES
|
NO
|
DRD2 S311C |
point mutation |
|
DRD2
|
5 (0/5/0) |
YES
|
YES
|
HTR2A -1438A/G |
point mutation |
|
HTR2A
|
4 (1/3/0) |
NO
|
YES
|
SERT VNTR |
VNTR |
|
SLC6A4
|
4 (2/2/0) |
YES
|
YES
|
ACE insertion/deletion |
insertion/deletion |
|
ACE
|
4 (2/2/0) |
YES
|
YES
|
KCNN3 exon 1 CAG-repeat |
microsatellite |
exon 1 |
KCNN3
|
4 (0/4/0) |
YES
|
NO
|
TH TaqI Polymorphism |
SNP |
|
TH
|
4 (2/2/0) |
NO
|
YES
|
MTHFR A1298C |
point mutation |
|
MTHFR
|
4 (3/1/0) |
YES
|
YES
|
rs6195 |
point mutation |
|
NR3C1
|
3 (0/3/0) |
NO
|
YES
|
HTR2A 516C/T |
point mutation |
|
HTR2A
|
3 (1/2/0) |
NO
|
NO
|
HTR2A His452Tyr |
point mutation |
|
HTR2A
|
3 (0/3/0) |
NO
|
NO
|
HTR2C Cys23Ser |
point mutation |
|
HTR2C
|
3 (3/0/0) |
NO
|
YES
|
BDNF 196G/A |
point mutation |
|
BDNF
|
3 (2/1/0) |
NO
|
NO
|
BDNF (GT)n |
microsatellite |
|
BDNF
|
3 (2/1/0) |
YES
|
YES
|
TCF4 CTG18.1 |
microsatellite |
|
TCF4
|
3 (1/2/0) |
YES
|
NO
|
TH PstI Polymorphism |
SNP |
|
TH
|
3 (0/3/0) |
NO
|
YES
|
WFS1 G576S |
point mutation |
exon8 |
WFS1
|
3 (0/3/0) |
NO
|
YES
|
WFS1 H611R |
point mutation |
exon8 |
WFS1
|
3 (0/3/0) |
NO
|
YES
|
MAOA RFLP |
point mutation |
|
MAOA
|
3 (1/2/0) |
NO
|
NO
|
MAOA T941G |
point mutation |
|
MAOA
|
3 (2/1/0) |
YES
|
YES
|
MAOB (GT)n |
microsatellite |
|
MAOB
|
3 (1/2/0) |
NO
|
YES
|
DAT VNTR |
VNTR |
|
SLC6A3
|
3 (0/3/0) |
NO
|
NO
|
DDC 1bp del |
insertion/deletion |
|
DDC
|
3 (2/1/0) |
NO
|
YES
|
XBP1 -116C>G |
point mutation |
|
XBP1
|
3 (1/2/0) |
NO
|
NO
|
DDC 4bp del |
insertion/deletion |
|
DDC
|
3 (1/2/0) |
NO
|
YES
|
DRD2 141ins/del |
insertion/deletion |
|
DRD2
|
3 (1/2/0) |
NO
|
NO
|
DRD2 TaqIA |
point mutation |
|
DRD2
|
3 (1/2/0) |
NO
|
NO
|
DRD2 TaqI Polymorphism |
SNP |
|
DRD2
|
3 (0/3/0) |
NO
|
NO
|
ERDA1 microsatellite |
microsatellite |
|
ERDA1
|
3 (0/3/0) |
YES
|
NO
|
NRG1 SNP8NRG241930 |
point mutation |
|
NRG1
|
3 (0/3/0) |
YES
|
NO
|
NRG1 SNP8NRG243177 |
point mutation |
|
NRG1
|
3 (0/3/0) |
YES
|
NO
|
GPR50 delta502-505 |
insertion/deletion |
|
GPR50
|
3 (1/2/0) |
YES
|
YES
|
GSK3B -1727A/T |
point mutation |
promoter |
GSK3B
|
3 (0/3/0) |
YES
|
NO
|
GSK3B -50T/C |
point mutation |
promoter |
GSK3B
|
3 (0/3/0) |
YES
|
NO
|
RGS4 SNP1 |
point mutation |
|
RGS4
|
2 (0/2/0) |
YES
|
NO
|
5-HT2A His452Tyr |
point mutation |
in the intracellular C-terminal end of the 5-HT2A protein |
HTR2A
|
2 (1/1/0) |
NO
|
NO
|
5-HT2A T102C |
point mutation |
|
HTR2A
|
2 (0/2/0) |
NO
|
NO
|
HTR2A Thr25Asn |
point mutation |
|
HTR2A
|
2 (0/2/0) |
NO
|
NO
|
ADCY9 2316A>G |
point mutation |
|
ADCY9
|
2 (1/1/0) |
NO
|
YES
|
ADCY9 (TTTA)n |
microsatellite |
|
ADCY9
|
2 (1/1/0) |
NO
|
YES
|
SLC6A3 -67A/T |
point mutation |
|
SLC6A3
|
2 (2/0/0) |
NO
|
NO
|
HTR6 267C/T |
point mutation |
|
HTR6
|
2 (1/1/0) |
YES
|
YES
|
IL1RN intron 2 VNTR |
VNTR |
intron 2 |
IL1RN
|
2 (1/1/0) |
YES
|
NO
|
IMPA2 -185A>G |
point mutation |
|
IMPA2
|
2 (0/2/0) |
YES
|
NO
|
IMPA2 -207T>C |
point mutation |
|
IMPA2
|
2 (2/0/0) |
YES
|
NO
|
SYBL1 intron5 G>C |
point mutation |
intron5 |
VAMP7
|
2 (0/2/0) |
NO
|
NO
|
IMPA2 443G>A (R148Q) |
point mutation |
|
IMPA2
|
2 (0/2/0) |
NO
|
NO
|
IMPA2 -461C>T |
point mutation |
|
IMPA2
|
2 (1/1/0) |
NO
|
NO
|
BDNF-LCPR |
microsatellite |
approximately 1.0 kb upstream of the translation initiation site of the BDNF gene |
BDNF
|
2 (1/1/0) |
NO
|
NO
|
IMPA2 -97-15G>A |
point mutation |
|
IMPA2
|
2 (0/2/0) |
NO
|
NO
|
TH BglII Polymorphism |
SNP |
|
TH
|
2 (2/0/0) |
NO
|
NO
|
COMT H/L |
others |
|
COMT
|
2 (1/1/0) |
NO
|
YES
|
TH TaqI RFLP |
RFLP |
|
TH
|
2 (1/1/0) |
NO
|
NO
|
TNF -G308A |
point mutation |
|
TNF
|
2 (1/1/0) |
YES
|
NO
|
TPH1 intron 7 218A/C |
SNP |
intron 7 |
TPH1
|
2 (0/2/0) |
NO
|
YES
|
DAT 40bp repeat |
duplication |
|
SLC6A3
|
2 (0/2/0) |
NO
|
YES
|
MAOA VNTR |
VNTR |
|
MAOA
|
2 (2/0/0) |
NO
|
NO
|
mtDNA A10398G |
point mutation |
|
mtDNA
|
2 (1/1/0) |
NO
|
NO
|
mtDNA C5178A |
point mutation |
|
mtDNA
|
2 (1/1/0) |
NO
|
NO
|
DRD1 1403T/C |
point mutation |
|
DRD1
|
2 (1/1/0) |
NO
|
NO
|
NDUFV2 -233T>C |
point mutation |
|
NDUFV2
|
2 (0/2/0) |
NO
|
NO
|
DRD1 -800T/C |
point mutation |
|
DRD1
|
2 (1/1/0) |
NO
|
NO
|
NDUFV2 -602G>A |
point mutation |
|
NDUFV2
|
2 (1/1/0) |
NO
|
NO
|
NDUFV2 -796C>G |
point mutation |
|
NDUFV2
|
2 (0/2/0) |
NO
|
NO
|
NDUFV2 86C>T |
point mutation |
|
NDUFV2
|
2 (0/2/0) |
NO
|
NO
|
DRD2 RFLP |
SNP |
|
DRD2
|
2 (0/2/0) |
NO
|
NO
|
DRD4 -521T/C |
point mutation |
|
DRD4
|
2 (0/2/0) |
NO
|
NO
|
NOS1 promoter VNTR |
VNTR |
promoter |
NOS1
|
2 (0/2/0) |
YES
|
NO
|
NOTCH4 (CTG)n |
microsatellite |
|
NOTCH4
|
2 (1/1/0) |
NO
|
NO
|
NRG1 420M9-1395 |
microsatellite |
|
NRG1
|
2 (0/2/0) |
NO
|
NO
|
NRG1 478B14-848 |
microsatellite |
|
NRG1
|
2 (0/2/0) |
NO
|
NO
|
NRG1 SNP8NRG221533 |
point mutation |
|
NRG1
|
2 (0/2/0) |
YES
|
NO
|
GRIN2B -200G/T |
point mutation |
|
GRIN2B
|
2 (0/2/0) |
YES
|
NO
|
PLA2 1-8 allele |
duplication |
|
PLA2G1B
|
2 (0/2/0) |
NO
|
NO
|
PLA2G1B microsatellite polymorphisms |
microsatellite |
|
PLA2G1B
|
2 (2/0/0) |
NO
|
NO
|
HARS TaqI Polymorphism |
SNP |
|
HARS
|
1 (0/1/0) |
NO
|
NO
|
PRODH-2026 |
point mutation |
|
PRODH
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2335301 -/G/A |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
HDAT-PCR1 |
SNP |
|
SLC6A3
|
1 (1/0/0) |
NO
|
NO
|
PRODH exon12 A472T |
point mutation |
exon12 |
PRODH
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2335333 -/ACACACAG/ACACACAC |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
218C10.CA44 |
microsatellite |
21q23 |
|
1 (0/1/0) |
NO
|
NO
|
hKCa CAG repeat |
duplication |
|
KCNN3
|
1 (0/1/0) |
NO
|
NO
|
PRODH exon12 R431H |
point mutation |
exon12 |
PRODH
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2335340 -/G/C |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
22A5.GT124 |
microsatellite |
21q23 |
|
1 (0/1/0) |
NO
|
NO
|
HLA-A polymorphism |
others |
|
HLA-A
|
1 (0/1/0) |
NO
|
NO
|
RFX4 D12S2072 |
microsatellite |
|
RFX4
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2336695 G/A |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
22CH3 CAG repeat |
microsatellite |
|
|
1 (1/0/0) |
YES
|
NO
|
HLA-B polymorphism |
others |
|
HLA-B
|
1 (0/1/0) |
NO
|
NO
|
RGS4 SNP18 |
point mutation |
|
RGS4
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2338101 -/TA/TATG |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
-2 bp deletion polymorphism |
insertion/deletion |
1 Mb apart from CHRNA7 |
CHRNA7
|
1 (1/0/0) |
NO
|
NO
|
HM74a GC09E01A |
point mutation |
|
HCAR2
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2338102 -/TG |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
314n7CA23 |
microsatellite |
21q23 |
|
1 (0/1/0) |
NO
|
NO
|
HM74a GC09E01B |
point mutation |
|
HCAR2
|
1 (0/1/0) |
NO
|
NO
|
RGS4 SNP4 |
point mutation |
|
RGS4
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2338946 G/A |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
314n7CA28 |
microsatellite |
21q23 |
|
1 (0/1/0) |
NO
|
NO
|
HM74 GC10E01A |
point mutation |
|
HCAR3
|
1 (0/1/0) |
NO
|
NO
|
RGS4 SNP7 |
point mutation |
|
RGS4
|
1 (1/0/0) |
YES
|
NO
|
CACNA1C Chr12:2339781 G/C |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
314n7CT18 |
microsatellite |
21q23 |
|
1 (0/1/0) |
NO
|
NO
|
HM74 GC10E01B |
point mutation |
|
HCAR3
|
1 (0/1/0) |
NO
|
NO
|
rs1129647 |
point mutation |
|
GABRA1
|
1 (1/0/0) |
NO
|
YES
|
CACNA1C Chr12:2341084 -/T |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
HM74 GC10E01C |
point mutation |
|
HCAR3
|
1 (0/1/0) |
NO
|
NO
|
rs1599988 |
point mutation |
|
mtDNA
|
1 (1/0/0) |
YES
|
NO
|
CACNA1C Chr12:2341393 -/G |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
5-HT2A promoter 1438A/G |
point mutation |
promoter |
HTR2A
|
1 (1/0/0) |
NO
|
NO
|
HM74 GC10E01D |
point mutation |
|
HCAR3
|
1 (0/1/0) |
NO
|
NO
|
rs28357375 |
point mutation |
|
mtDNA
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2341397 G/T |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
HM74 GC10E01E |
point mutation |
|
HCAR3
|
1 (0/1/0) |
NO
|
NO
|
rs28357968 |
point mutation |
|
mtDNA
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2347245 -/TT |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
5-HTR2C RFLP |
SNP |
|
HTR2C
|
1 (0/1/0) |
NO
|
NO
|
HTR1A (CA)n/(GT)n 10 |
duplication |
|
HTR1A
|
1 (0/1/0) |
NO
|
NO
|
rs2853515 |
point mutation |
|
mtDNA
|
1 (1/0/0) |
YES
|
NO
|
CACNA1C Chr12:2349920 -/TGGCCTCCTCA |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
HTR1B G861C |
point mutation |
|
HTR1B
|
1 (0/1/0) |
NO
|
NO
|
rs3937033 |
point mutation |
|
mtDNA
|
1 (1/0/0) |
YES
|
NO
|
CACNA1C Chr12:2349920 GTGGCCTCCTCAT/GT |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
HTR1B T371G |
point mutation |
|
HTR1B
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2352902 G/A |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
5-HTT PstI RFLP |
SNP |
|
SLC6A4
|
1 (0/1/0) |
NO
|
NO
|
HTR1D HincII Polymorphism |
SNP |
|
HTR1D
|
1 (0/1/0) |
NO
|
NO
|
rs6414684 |
point mutation |
|
GABRB1
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2354984 C/T |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
AADC exon 1 T>A |
point mutation |
exon 1 |
DDC
|
1 (0/1/0) |
YES
|
NO
|
HTR1D TaqI Polymorphism |
SNP |
|
HTR1D
|
1 (0/1/0) |
NO
|
NO
|
rs769404 |
point mutation |
|
GAD1
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2362014 G/C |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCA13 exon33 H3609P |
point mutation |
exon33 |
ABCA13
|
1 (0/1/0) |
YES
|
YES
|
HTR2A 1018578T/G |
point mutation |
|
HTR2A
|
1 (0/1/0) |
NO
|
NO
|
rs854560 |
point mutation |
|
PON1
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2365088 G/T |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCA13 exon40 T4031A |
point mutation |
exon40 |
ABCA13
|
1 (1/0/0) |
YES
|
YES
|
HTR2A 1018579A/G |
point mutation |
|
HTR2A
|
1 (0/1/0) |
NO
|
NO
|
RSN GC04E12A |
point mutation |
|
CLIP1
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2365131 C/T |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCA13 exon52 R4590W |
point mutation |
exon52 |
ABCA13
|
1 (0/1/0) |
YES
|
YES
|
HTR2A 1354C/T |
point mutation |
|
HTR2A
|
1 (1/0/0) |
NO
|
NO
|
RSN GC04E14A |
point mutation |
|
CLIP1
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2370397 -/A |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCA13 exon52 T4550A |
point mutation |
exon52 |
ABCA13
|
1 (1/0/0) |
YES
|
YES
|
HTR2A 1360020G/T |
point mutation |
|
HTR2A
|
1 (0/1/0) |
NO
|
NO
|
RSN GC04E19A |
point mutation |
|
CLIP1
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2370911 -/ACACAC |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCA13 exon54 R4728X |
point mutation |
exon54 |
ABCA13
|
1 (0/1/0) |
YES
|
YES
|
S100B-HaeIII |
microsatellite |
21q22.3 |
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2375362 -/TT |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCA13 exon57 R4843C |
point mutation |
exon57 |
ABCA13
|
1 (0/1/0) |
YES
|
YES
|
HTR2A 1854352A/G |
point mutation |
|
HTR2A
|
1 (0/1/0) |
NO
|
NO
|
SBNO1 GC22E16A |
point mutation |
|
SBNO1
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2381652 G/A |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCG1 1248+14insC |
insertion/deletion |
|
ABCG1
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2385027 -/A |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCG1 1249-64G>T |
point mutation |
|
ABCG1
|
1 (0/1/0) |
NO
|
NO
|
HTR2A 74C/A |
point mutation |
|
HTR2A
|
1 (0/1/0) |
NO
|
NO
|
SCYA2 A-2518G |
point mutation |
promoter |
CCL2
|
1 (1/0/0) |
NO
|
YES
|
CACNA1C Chr12:2385246 G/T |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCG1 274+11C>T |
point mutation |
|
ABCG1
|
1 (0/1/0) |
NO
|
NO
|
HTR2A BbvI Polymorphism |
SNP |
|
HTR2A
|
1 (0/1/0) |
NO
|
NO
|
SEF2-1B |
microsatellite |
|
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2389778 G/A |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCG1 -533A>G |
point mutation |
|
ABCG1
|
1 (0/1/0) |
NO
|
NO
|
SERT insertion/deletion |
insertion/deletion |
|
SLC6A4
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2391029 -/T |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCG1 576+139A>G |
point mutation |
|
ABCG1
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2392186 -/T |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCG1 723-20C>T |
point mutation |
|
ABCG1
|
1 (0/1/0) |
NO
|
NO
|
HTR2A HpaII Polymorphism |
point mutation |
|
HTR2A
|
1 (0/1/0) |
NO
|
NO
|
SLC12A6 32416574(G/A) |
point mutation |
|
SLC12A6
|
1 (1/0/0) |
YES
|
NO
|
CACNA1C Chr12:2418658 -/AC |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCG1 -768G>A |
point mutation |
|
ABCG1
|
1 (0/1/0) |
NO
|
NO
|
HTR2A MspI Polymorphism |
SNP |
|
HTR2A
|
1 (1/0/0) |
NO
|
NO
|
SLC12A6 32418760(G/A) |
point mutation |
|
SLC12A6
|
1 (1/0/0) |
YES
|
NO
|
CACNA1C Chr12:2418658 -/T/TAC |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCG1 A2424G |
point mutation |
|
ABCG1
|
1 (0/1/0) |
NO
|
NO
|
SLC12A6 IVS4+1008ins(T)/del(T) |
insertion/deletion |
|
SLC12A6
|
1 (1/0/0) |
YES
|
NO
|
CACNA1C Chr12:2418659 AC/ACAC |
duplication |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCG1 D21S1225 |
microsatellite |
|
ABCG1
|
1 (1/0/0) |
NO
|
NO
|
SLC1A4-11 |
microsatellite |
|
SLC1A4
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2419508 -/A |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCG1 I6 61VNTR |
VNTR |
|
ABCG1
|
1 (0/1/0) |
NO
|
NO
|
HTR2C GT(12-18)/CT(4-5) |
microsatellite |
|
HTR2C
|
1 (0/1/0) |
NO
|
NO
|
SLC6A3 1342A/G |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2419516 A/T/AAT |
point mutation/duplication |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ABCG1 UTR poly(T) |
VNTR |
|
ABCG1
|
1 (0/1/0) |
NO
|
NO
|
HTR2C HinfI Polymorphism |
SNP |
|
HTR2C
|
1 (1/0/0) |
NO
|
NO
|
SLC6A3 1398-21G/A |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2421980 -/T |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ACE1 dbSNP4295 |
point mutation |
|
ACE
|
1 (0/1/0) |
NO
|
NO
|
HTR3A C178T |
point mutation |
|
HTR3A
|
1 (1/0/0) |
NO
|
NO
|
SLC6A3 1398-56A/G |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2423175 G/C |
point mutation |
Intron |
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
HTR3A C195T |
point mutation |
|
HTR3A
|
1 (0/1/0) |
NO
|
NO
|
SLC6A3 1436209 C>G |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2694668 G/A |
point mutation |
Splice site |
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ADARB1 c.2234A>G |
point mutation |
exon10 |
ADARB1
|
1 (0/1/0) |
NO
|
NO
|
HTR3A exon1 Leu10Leu |
point mutation |
exon1 |
HTR3A
|
1 (0/1/0) |
YES
|
NO
|
SLC6A3 1626+14G/A |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2788668 C/G |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
HTR3A exon3 A(+7 IVS3)C |
point mutation |
exon3 |
HTR3A
|
1 (0/1/0) |
YES
|
NO
|
SLC6A3 1859C/T |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2800689 A/G |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
HTR3A exon6 Leu192Leu |
point mutation |
exon6 |
HTR3A
|
1 (0/1/0) |
YES
|
NO
|
SLC6A3 1967+29insTC |
insertion/deletion |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2800954 GCACGGGCCACGCCGAGCTCCCGGCCA/- |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ADCYAP1 IVS3 37A/T |
point mutation |
|
ADCYAP1
|
1 (0/1/0) |
YES
|
NO
|
HTR3A exon7 Lys277Lys |
point mutation |
exon7 |
HTR3A
|
1 (0/1/0) |
YES
|
NO
|
SLC6A3 242C/T |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2801016 C/G/CGCCGCCGGGAAGGG |
point mutation/insertion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ADRA1A 492C>T |
point mutation |
exon 2 |
ADRA1A
|
1 (0/1/0) |
NO
|
NO
|
HTR3A exon8 Arg344His |
point mutation |
exon8 |
HTR3A
|
1 (0/1/0) |
YES
|
NO
|
SLC6A3 3'UTR VNTR |
VNTR |
3'UTR |
SLC6A3
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2801133 T/A |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ADRA1B hcv1738292 |
point mutation |
|
ADRA1B
|
1 (1/0/0) |
NO
|
NO
|
HTR3A exon9 Leu459Leu |
point mutation |
exon9 |
HTR3A
|
1 (0/1/0) |
YES
|
NO
|
SLC6A3 547-12C/A |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2803097 T/G |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ADRA2A -1291C>G |
point mutation |
|
ADRA2A
|
1 (0/1/0) |
NO
|
NO
|
HTR3A exon9 Pro391Arg |
point mutation |
exon9 |
HTR3A
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2804191 T/G |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ADRA2C 5'UTR (GT)n |
microsatellite |
5' UTR |
ADRA2C
|
1 (0/1/0) |
NO
|
NO
|
HTR3B 386A>C (Tyr129Ser) |
point mutation |
|
HTR3B
|
1 (1/0/0) |
YES
|
NO
|
SLC6A3 Ala559Val |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2804268 T/- |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
AGAT10 |
microsatellite |
21q23 |
|
1 (0/1/0) |
NO
|
NO
|
HTR3B 547G>A (Val183Ile) |
point mutation |
|
HTR3B
|
1 (1/0/0) |
YES
|
NO
|
SLC6A3 Glu602Gly |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2804832 G/- |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
AGT M235T |
point mutation |
|
AGT
|
1 (1/0/0) |
NO
|
NO
|
HTR3B 5'UTR -102delAAG |
insertion/deletion |
5'UTR |
HTR3B
|
1 (1/0/0) |
YES
|
NO
|
SLC6A3 I11+2478 |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2806546 G/A |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
ALDH2 *1/*2 |
point mutation |
|
ALDH2
|
1 (1/0/0) |
NO
|
NO
|
HTR3B IVS4+11C>T |
point mutation |
|
HTR3B
|
1 (0/1/0) |
YES
|
NO
|
SLC6A3 I12+268 |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
MTHFR exon 4 C677T |
SNP |
exon 4 |
MTHFR
|
1 (1/0/0) |
YES
|
NO
|
ALDH2 *1*2 allele |
others |
|
ALDH2
|
1 (0/1/0) |
NO
|
NO
|
HTR3B IVS4+12G>A |
point mutation |
|
HTR3B
|
1 (0/1/0) |
YES
|
NO
|
SLC6A3 I13+1457 |
point mutation |
|
SLC6A3
|
1 (1/0/0) |
NO
|
NO
|
MTHFR exon 7 A1298C |
SNP |
exon 7 |
MTHFR
|
1 (1/0/0) |
YES
|
NO
|
ALG9 D11S5025 |
microsatellite |
|
ALG9
|
1 (0/1/0) |
NO
|
NO
|
HTR3B IVS6+72A>G |
point mutation |
|
HTR3B
|
1 (0/1/0) |
YES
|
NO
|
SLC6A3 I14+4217 |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
GRM7 3 6900524 1000G |
deletion |
Promoter |
GRM7
|
1 (0/1/0) |
NO
|
NO
|
ALG9 D11S5026 |
microsatellite |
|
ALG9
|
1 (0/1/0) |
NO
|
NO
|
HTR4 IVS1+15T/C |
point mutation |
|
HTR4
|
1 (0/1/0) |
YES
|
YES
|
SLC6A3 I5+448 |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
GRM7 3 6901914 1000G |
deletion |
Promoter |
GRM7
|
1 (0/1/0) |
NO
|
NO
|
ALG9 D11S5027 |
microsatellite |
|
ALG9
|
1 (0/1/0) |
NO
|
NO
|
HTR4 IVS3+63C/T |
point mutation |
|
HTR4
|
1 (0/1/0) |
YES
|
YES
|
SLC6A3 I7+922 |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
GRM7 3 6902624 1000G |
insertion |
Promoter |
GRM7
|
1 (0/1/0) |
NO
|
NO
|
ALG9 D11S5028 |
microsatellite |
|
ALG9
|
1 (0/1/0) |
NO
|
NO
|
HTR4 IVS3+6G/A |
point mutation |
|
HTR4
|
1 (0/1/0) |
YES
|
YES
|
SLC6A3 I8+2086 |
point mutation |
|
SLC6A3
|
1 (1/0/0) |
NO
|
NO
|
GRM7 3f 7313045 |
point mutation |
Promoter of ENST00000463676 isoform |
GRM7
|
1 (0/1/0) |
NO
|
NO
|
ALOX12 R261Q |
point mutation |
|
ALOX12
|
1 (1/0/0) |
NO
|
NO
|
HTR4 IVS4+36T/C |
point mutation |
|
HTR4
|
1 (0/1/0) |
YES
|
YES
|
SLC6A3 P+2459 |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
GRM7 nPb 7467774 |
point mutation |
Promoter of ENST00000458641 isoform |
GRM7
|
1 (0/1/0) |
NO
|
NO
|
alpha8-alpha10 del |
insertion/deletion |
16.7-kb deletion affecting PCDH-alpha exons 8-10 |
5q31-linked PCDH family
|
1 (0/1/0) |
YES
|
NO
|
HTR4 SVRSNP1 |
point mutation |
|
HTR4
|
1 (1/0/0) |
YES
|
YES
|
SLC6A4 3'UTR G/T |
point mutation |
3'UTR |
SLC6A4
|
1 (0/1/0) |
NO
|
NO
|
GRM7 nPa 7493030 |
indel |
Promoter of ENST00000458641 isoform |
GRM7
|
1 (0/1/0) |
NO
|
NO
|
APOE e3/e4 |
point mutation |
|
APOE
|
1 (1/0/0) |
NO
|
NO
|
HTR4 SVRSNP2 |
point mutation |
|
HTR4
|
1 (1/0/0) |
YES
|
YES
|
SLC6A5 AC-tandem-repeat |
microsatellite |
|
SLC6A5
|
1 (0/1/0) |
YES
|
NO
|
GRM7 nex4 7600830 |
indel |
Exon of ENST00000458641 isoform |
GRM7
|
1 (0/1/0) |
NO
|
NO
|
ATP1A3 2-7 allele |
others |
|
ATP1A3
|
1 (1/0/0) |
NO
|
NO
|
HTR4 SVRSNP3 |
point mutation |
|
HTR4
|
1 (1/0/0) |
YES
|
YES
|
SNAP25 promoter SNP1 |
point mutation |
promoter |
SNAP25
|
1 (0/1/0) |
NO
|
NO
|
GRM7 nex7 7649745 |
insertion |
Exon of ENST00000458641 isoform |
GRM7
|
1 (0/1/0) |
NO
|
NO
|
ATP1B3 4E12 |
microsatellite |
|
ATP1B3
|
1 (0/1/0) |
NO
|
NO
|
HTR4 SVRSNP4 |
point mutation |
|
HTR4
|
1 (1/0/0) |
YES
|
YES
|
SNAP29 exon1 56T>C |
point mutation |
exon1 |
SNAP29
|
1 (0/1/0) |
YES
|
NO
|
GRM7 nex8 7678357 |
point mutation |
Exon of ENST00000458641 isoform |
GRM7
|
1 (0/1/0) |
NO
|
NO
|
ATP2A2 exon15 2172G/A |
point mutation |
exon15 |
ATP2A2
|
1 (0/1/0) |
NO
|
NO
|
HTR5A 12A/T |
point mutation |
|
HTR5A
|
1 (0/1/0) |
NO
|
YES
|
SNAP29 exon1 92A>G |
point mutation |
exon1 |
SNAP29
|
1 (0/1/0) |
YES
|
NO
|
GRM7 9c 7698252 |
point mutation |
Exon 9 3' UTR |
GRM7
|
1 (0/1/0) |
NO
|
NO
|
ATP2A2 exon15 2295G/A |
point mutation |
exon15 |
ATP2A2
|
1 (0/1/0) |
NO
|
NO
|
HTR5A 19G/C |
point mutation |
|
HTR5A
|
1 (0/1/0) |
NO
|
YES
|
SNAP29 promoter -849G>A |
point mutation |
promoter |
SNAP29
|
1 (0/1/0) |
YES
|
NO
|
STR |
Simple T repeat |
Exon 9 3' UTR |
GRM7
|
1 (0/1/0) |
NO
|
NO
|
ATP2A2 exon18 2697G/T |
point mutation |
exon18 |
ATP2A2
|
1 (0/1/0) |
NO
|
NO
|
HTR6 126G/T |
point mutation |
|
HTR6
|
1 (0/1/0) |
YES
|
NO
|
SOD2 Ala-9Val |
point mutation |
|
SOD2
|
1 (0/1/0) |
NO
|
YES
|
GRM7 Ex14 Indel |
insertion |
Exon 14 |
GRM7
|
1 (0/1/0) |
NO
|
NO
|
ATP2A2 exon1 87C/T |
point mutation |
exon1 |
ATP2A2
|
1 (0/1/0) |
NO
|
NO
|
SSTR5 -2134delT |
insertion/deletion |
|
SSTR5
|
1 (0/1/0) |
NO
|
NO
|
TACR1 ss825678898 |
insertion/deletion |
|
TACR1
|
1 (0/1/0) |
NO
|
NO
|
ATP2A2 intron3 220-18G/A |
point mutation |
intron3 |
ATP2A2
|
1 (0/1/0) |
NO
|
NO
|
HTR6 873+128A/C |
point mutation |
|
HTR6
|
1 (1/0/0) |
YES
|
NO
|
SSTR5 A-1665G |
point mutation |
|
SSTR5
|
1 (0/1/0) |
NO
|
NO
|
TACR1 Chr2:75280719:D |
insertion/deletion |
Regulatory region: ENSR00000676664; Intronic: ENST00000409848, ENST00000305249 |
TACR1
|
1 (1/0/0) |
NO
|
NO
|
ATP2A2 promoter -2549G/A |
point mutation |
promoter |
ATP2A2
|
1 (0/1/0) |
NO
|
NO
|
HTR6 873+30C/T |
point mutation |
|
HTR6
|
1 (0/1/0) |
NO
|
NO
|
SSTR5 C1004T |
point mutation |
|
SSTR5
|
1 (1/0/0) |
NO
|
NO
|
TACR1 Chr2:75327565:D |
insertion/deletion |
Regulatory region: ENSR00001543768; Intronic: ENST00000409848, ENST00000305249 |
TACR1
|
1 (1/0/0) |
NO
|
NO
|
ATTT11 |
microsatellite |
21q23 |
|
1 (0/1/0) |
NO
|
NO
|
HTR7 XhoI Polymorphism |
SNP |
|
HTR7
|
1 (0/1/0) |
NO
|
NO
|
SSTR5 C142A |
point mutation |
|
SSTR5
|
1 (1/0/0) |
NO
|
NO
|
TACR1 Chr2:75339547:D |
insertion/deletion |
Intronic: ENST00000409848, ENST00000305249 |
TACR1
|
1 (1/0/0) |
NO
|
NO
|
BDNF 11757C/G |
point mutation |
|
BDNF
|
1 (1/0/0) |
NO
|
NO
|
IFNG 874T/A |
point mutation |
|
IFNG
|
1 (1/0/0) |
NO
|
NO
|
SSTR5 C155T |
point mutation |
|
SSTR5
|
1 (0/1/0) |
NO
|
NO
|
TACR1 Chr2:75359623:D |
insertion/deletion |
Intronic: ENST00000409848, ENST00000305249 |
TACR1
|
1 (1/0/0) |
NO
|
NO
|
BDNF 12910C/A |
point mutation |
|
BDNF
|
1 (0/1/0) |
NO
|
NO
|
IGF1 (CA)n |
microsatellite |
|
IGF1
|
1 (1/0/0) |
NO
|
NO
|
SSTR5 C325T |
point mutation |
|
SSTR5
|
1 (0/1/0) |
NO
|
NO
|
chr2:75561695:D |
insertion/deletion |
Intergenic variant |
|
1 (1/0/0) |
NO
|
NO
|
BDNF -1360C>T |
point mutation |
|
BDNF
|
1 (0/1/0) |
NO
|
NO
|
IL10 1082G/A |
point mutation |
|
IL10
|
1 (0/1/0) |
NO
|
YES
|
SSTR5 C633T |
point mutation |
|
SSTR5
|
1 (0/1/0) |
NO
|
NO
|
chr2:75618722:I |
insertion/deletion |
Intergenic variant |
|
1 (1/0/0) |
NO
|
NO
|
BDNF 14569G/A |
point mutation |
|
BDNF
|
1 (1/0/0) |
NO
|
NO
|
SSTR5 C-801G |
point mutation |
|
SSTR5
|
1 (0/1/0) |
NO
|
NO
|
EVA1A chr2:75693696:D |
insertion/deletion |
Downstream of ENST00000485891, ENST00000490746 |
EVA1A
|
1 (1/0/0) |
NO
|
NO
|
BDNF -1480C/G |
point mutation |
|
BDNF
|
1 (0/1/0) |
NO
|
NO
|
IL6 174G/C |
point mutation |
|
IL6
|
1 (0/1/0) |
NO
|
NO
|
SSTR5 G573A |
point mutation |
|
SSTR5
|
1 (1/0/0) |
NO
|
NO
|
rs63470962 |
insertion |
|
GRM7
|
1 (0/1/0) |
NO
|
NO
|
IMPA2 159T>C |
point mutation |
|
IMPA2
|
1 (1/0/0) |
NO
|
NO
|
SSTR5 T-2187G |
point mutation |
|
SSTR5
|
1 (0/1/0) |
NO
|
NO
|
rs113329024 |
insertion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
BDNF 3071G/A |
point mutation |
|
BDNF
|
1 (0/1/0) |
NO
|
NO
|
SSTR5 T-461C |
point mutation |
|
SSTR5
|
1 (0/1/0) |
NO
|
NO
|
MIR137/MIR2682 Chr1:98515539 A/T |
point mutation |
Enhancer |
MIR137, MIR2682
|
1 (1/0/0) |
YES
|
NO
|
BDNF -633T/A |
point mutation |
|
BDNF
|
1 (1/0/0) |
NO
|
NO
|
SLC1A2 Chr1:35441380 G/C |
point mutation |
Putative promoter |
SLC1A2
|
1 (0/1/0) |
NO
|
NO
|
BDNF 9202G/A |
point mutation |
|
BDNF
|
1 (0/1/0) |
NO
|
NO
|
IMPA2 230+141G>A |
point mutation |
|
IMPA2
|
1 (0/1/0) |
NO
|
NO
|
SYNGR1 exon3 Ser97Ser |
point mutation |
exon3 |
SYNGR1
|
1 (1/0/0) |
YES
|
NO
|
SLC1A2 Chr1:35440927 A/G |
point mutation |
5'-UTR |
SLC1A2
|
1 (0/1/0) |
NO
|
NO
|
BDNF A-633T |
point mutation |
|
BDNF
|
1 (0/1/0) |
NO
|
NO
|
IMPA2 -241 -237dup |
duplication |
|
IMPA2
|
1 (0/1/0) |
NO
|
NO
|
SYNGR1 exon6 Asn(ins/del) |
insertion/deletion |
exon6 |
SYNGR1
|
1 (0/1/0) |
YES
|
NO
|
SLC1A2 Chr1:35440635 G/A |
point mutation |
5'-UTR |
SLC1A2
|
1 (0/1/0) |
NO
|
NO
|
BDNF C270T |
point mutation |
|
BDNF
|
1 (0/1/0) |
NO
|
NO
|
IMPA2 382-44G>A |
point mutation |
|
IMPA2
|
1 (0/1/0) |
NO
|
NO
|
SYNJ1 intron12 IVS12+15delT,+17delT |
insertion/deletion |
intron12 |
SYNJ1
|
1 (0/1/0) |
NO
|
NO
|
SLC1A2 Chr1:35440563 C/G |
point mutation |
5'-UTR |
SLC1A2
|
1 (0/1/0) |
NO
|
NO
|
BDNF (CA) |
microsatellite |
1.3 kb away from rs6265 |
BDNF
|
1 (0/1/0) |
NO
|
NO
|
SYNJ1 IVS12+15delT,+17delT |
insertion/deletion |
|
SYNJ1
|
1 (0/1/0) |
NO
|
NO
|
SLC1A2 Chr1:35344202 G/T |
point mutation |
Exonic p.(A20S) 5'-UTR |
SLC1A2
|
1 (0/1/0) |
YES
|
NO
|
BDNF g.11757C>G |
point mutation |
|
BDNF
|
1 (0/1/0) |
NO
|
NO
|
SYNJ1 IVS28-7G/T |
point mutation |
|
SYNJ1
|
1 (0/1/0) |
NO
|
NO
|
SLC1A2 Chr1:35339061 C/T |
point mutation |
Exonic p.(A7V) |
SLC1A2
|
1 (0/1/0) |
YES
|
NO
|
IMPA2 490+13 14insA |
insertion/deletion |
|
IMPA2
|
1 (0/1/0) |
NO
|
NO
|
SYNJ1 IVS29+14C/T |
point mutation |
|
SYNJ1
|
1 (0/1/0) |
NO
|
NO
|
SLC1A2 Chr1:35282452 C/T |
point mutation |
Exonic p.(R572C) |
SLC1A2
|
1 (0/1/0) |
YES
|
NO
|
BDNF hCV11592756 |
point mutation |
|
BDNF
|
1 (1/0/0) |
NO
|
NO
|
IMPA2 599+97G>A |
point mutation |
|
IMPA2
|
1 (0/1/0) |
NO
|
NO
|
SYNJ1 K295R |
point mutation |
|
SYNJ1
|
1 (0/1/0) |
NO
|
NO
|
SLC1A2 Chr1:35279202 A/G |
point mutation |
3'-UTR |
SLC1A2
|
1 (0/1/0) |
NO
|
NO
|
IMPA2 599+99G>A |
point mutation |
|
IMPA2
|
1 (0/1/0) |
NO
|
NO
|
TBP CAG/CAA repeats |
microsatellite |
|
TBP
|
1 (0/1/0) |
NO
|
NO
|
IL1B Chr2:113304498 |
|
Exonic |
IL1B
|
1 (0/0/1) |
NO
|
NO
|
IMPA2 -708G>A |
point mutation |
|
IMPA2
|
1 (0/1/0) |
YES
|
NO
|
TBX1 v14186 |
point mutation |
|
TBX1
|
1 (0/1/0) |
YES
|
YES
|
IL36RN Chr2:113536607 |
|
Exonic |
IL36RN
|
1 (0/0/1) |
NO
|
NO
|
C21ORF2 |
insertion/deletion |
21q23 |
|
1 (0/1/0) |
NO
|
NO
|
TCF4 CAG/CTG repeat |
microsatellite |
|
TCF4
|
1 (0/1/0) |
NO
|
NO
|
IL1RN Chr2:113594121 |
|
Intronic, Exonic |
IL1RN
|
1 (0/0/1) |
NO
|
NO
|
CAP2 triplet repeat |
microsatellite |
|
CAP2
|
1 (0/1/0) |
NO
|
NO
|
IMPA2 IVS1-15G>A |
point mutation |
|
IMPA2
|
1 (0/1/0) |
YES
|
NO
|
ACTR3 Chr2:114401422 |
|
Exonic |
ACTR3
|
1 (0/0/1) |
NO
|
NO
|
CCK STR |
microsatellite |
|
CCK
|
1 (0/1/0) |
NO
|
YES
|
IMPA2 IVS5+13-14InsA |
insertion/deletion |
|
IMPA2
|
1 (0/1/0) |
YES
|
NO
|
TH 1-5 allele |
others |
|
TH
|
1 (0/1/0) |
NO
|
YES
|
DPP10 Chr2:116251310 |
|
Exonic |
DPP10
|
1 (0/0/1) |
NO
|
NO
|
CD18-AciI |
microsatellite |
21q22.3 |
|
1 (0/1/0) |
NO
|
NO
|
INPP1 C973A |
point mutation |
|
INPP1
|
1 (0/1/0) |
NO
|
NO
|
DPP10 Chr2:116314867 |
|
Exonic |
DPP10
|
1 (0/0/1) |
NO
|
NO
|
CHRFAM7A 2bp deletion |
insertion/deletion |
|
CHRFAM7A
|
1 (0/1/0) |
YES
|
NO
|
INS PvuII Polymorphism |
SNP |
|
INS
|
1 (0/1/0) |
NO
|
NO
|
TH BglII |
RFLP |
|
TH
|
1 (1/0/0) |
NO
|
NO
|
PTPN4 Chr2:120419158 |
|
Exonic |
PTPN4
|
1 (0/0/1) |
NO
|
NO
|
CHRNA7 -86C/T |
point mutation |
|
CHRNA7
|
1 (0/1/0) |
NO
|
NO
|
iPLA2 C/T |
point mutation |
|
PLA2G6
|
1 (0/1/0) |
NO
|
NO
|
TH (CATT)n |
duplication |
|
TH
|
1 (1/0/0) |
NO
|
NO
|
GLI2 Chr2:121444612 |
|
Exonic |
GLI2
|
1 (0/0/1) |
NO
|
NO
|
COL6A1 |
VNTR |
21q23 |
|
1 (0/1/0) |
NO
|
NO
|
KAT5 BanI polymorphism |
point mutation |
|
KAT5
|
1 (0/1/0) |
NO
|
YES
|
TH intron 1 tetranucleotide polymorphism |
others |
intron 1 |
TH
|
1 (0/1/0) |
NO
|
NO
|
GLI2 Chr2:121464518 |
|
Exonic |
GLI2
|
1 (0/0/1) |
NO
|
NO
|
COMT C256G |
SNP |
|
COMT
|
1 (0/1/0) |
NO
|
NO
|
KCNN3 CAG/CTG repeat |
microsatellite |
1q21.3 |
KCNN3
|
1 (0/1/0) |
NO
|
NO
|
ZHX1 Chr8:124336277 |
|
Intronic, Exonic, ncRNA |
ZHX1-C8orf76, ZHX1
|
1 (0/0/1) |
NO
|
NO
|
COMT Codon108/158 |
point mutation |
|
COMT
|
1 (0/1/0) |
NO
|
NO
|
ZHX1 Chr8:124336599 |
|
Intronic, Exonic, ncRNA |
ZHX1-C8orf76, ZHX1
|
1 (0/0/1) |
NO
|
NO
|
COMT G/A |
point mutation |
|
COMT
|
1 (1/0/0) |
NO
|
YES
|
KCNQ2 3'end 30-15/54 |
point mutation |
3'end |
KCNQ2
|
1 (0/1/0) |
NO
|
NO
|
ATAD2 Chr8:124419211 |
|
Exonic |
ATAD2
|
1 (0/0/1) |
NO
|
NO
|
KCNQ2 3'end 30-84/37 |
point mutation |
3'end |
KCNQ2
|
1 (0/1/0) |
NO
|
NO
|
ATAD2 Chr8:124440660 |
|
Exonic |
ATAD2
|
1 (0/0/1) |
NO
|
NO
|
COMT NlaIII |
point mutation |
|
COMT
|
1 (1/0/0) |
NO
|
NO
|
KCNQ2 5'end 4/30/1958 |
point mutation |
5'end |
KCNQ2
|
1 (0/1/0) |
NO
|
NO
|
TH (TCAT)n |
microsatellite |
|
TH
|
1 (0/1/0) |
YES
|
NO
|
ATAD2 Chr8:124451340 |
|
Exonic |
ATAD2
|
1 (0/0/1) |
NO
|
NO
|
COMT P2 promoter -278A/G |
point mutation |
P2 promoter |
COMT
|
1 (0/1/0) |
NO
|
NO
|
KCNQ2 Intron12 7/30/1930 |
point mutation |
Intron12 |
KCNQ2
|
1 (1/0/0) |
NO
|
NO
|
TH tetranucleotide repeat |
tetranucleotide repeat |
|
TH
|
1 (0/1/0) |
NO
|
NO
|
FBXO32 Chr8:124614644 |
|
Exonic |
FBXO32
|
1 (0/0/1) |
NO
|
NO
|
KCNQ2 Intron 30-2/62 |
point mutation |
Intron |
KCNQ2
|
1 (1/0/0) |
NO
|
NO
|
TH VNTR |
VNTR |
|
TH
|
1 (0/1/0) |
NO
|
NO
|
TRIB1 Chr8:126514759 |
|
Exonic |
TRIB1
|
1 (0/0/1) |
NO
|
NO
|
cPLA2 BanI dimorphic site |
point mutation |
|
KAT5
|
1 (0/1/0) |
NO
|
NO
|
KCNQ2 Intron4 30-17/37 |
point mutation |
Intron4 |
KCNQ2
|
1 (0/1/0) |
NO
|
NO
|
ATP6V0A2 TJ6 GC24E19A |
point mutation |
|
ATP6V0A2
|
1 (0/1/0) |
NO
|
NO
|
MYC Chr8:128819709 |
|
Exonic |
MYC
|
1 (0/0/1) |
NO
|
NO
|
CRH polymorphisms |
VNTR |
|
CRH
|
1 (0/1/0) |
NO
|
NO
|
KIAA1595 GC29E04A |
point mutation |
|
DDX55
|
1 (0/1/0) |
NO
|
NO
|
TMEM1 microsatellite |
microsatellite |
21q22.3 |
TRAPPC10
|
1 (0/1/0) |
NO
|
NO
|
DYNC1H1 Chr14:101530331 |
|
Exonic |
DYNC1H1
|
1 (0/0/1) |
NO
|
NO
|
CRHR2 1047G/A |
point mutation |
|
CRHR2
|
1 (0/1/0) |
NO
|
YES
|
KIAA1595 GC29E06A |
point mutation |
|
DDX55
|
1 (1/0/0) |
NO
|
NO
|
TNF-alpha 308G/A |
point mutation |
|
TNF
|
1 (1/0/0) |
NO
|
NO
|
DYNC1H1 Chr14:101533297 |
|
Exonic |
DYNC1H1
|
1 (0/0/1) |
NO
|
NO
|
CRHR2 intron10 (GAT)n |
microsatellite |
intron10 |
CRHR2
|
1 (1/0/0) |
NO
|
NO
|
KIAA1595 GC29E08A |
point mutation |
|
DDX55
|
1 (0/1/0) |
NO
|
NO
|
HSP90AA1 Chr14:101622401 |
|
Exonic |
HSP90AA1
|
1 (0/0/1) |
NO
|
NO
|
CRHR2 intron10 (GT)n |
microsatellite |
intron10 |
CRHR2
|
1 (0/1/0) |
NO
|
NO
|
KNTC1 GC07E08A |
point mutation |
|
KNTC1
|
1 (0/1/0) |
NO
|
NO
|
TPH1 3'UTR A27237G |
point mutation |
3'UTR |
TPH1
|
1 (0/1/0) |
NO
|
NO
|
RCOR1 Chr14:102250649 |
|
Exonic |
RCOR1
|
1 (0/0/1) |
NO
|
NO
|
CRHR2 intron4 (CA)n |
microsatellite |
intron4 |
CRHR2
|
1 (0/1/0) |
NO
|
NO
|
KNTC1 GC07E25A |
point mutation |
|
KNTC1
|
1 (0/1/0) |
NO
|
NO
|
TPH1 5'flanking A-1067G |
point mutation |
5'flanking |
TPH1
|
1 (0/1/0) |
NO
|
NO
|
MARK3 Chr14:102985013 |
|
Exonic |
MARK3
|
1 (0/0/1) |
NO
|
NO
|
CUX2 1191C/T |
point mutation |
|
CUX2
|
1 (0/1/0) |
NO
|
NO
|
KNTC1 GC07E57A |
point mutation |
|
KNTC1
|
1 (0/1/0) |
NO
|
NO
|
TPH1 5'flanking G-347T |
point mutation |
5'flanking |
TPH1
|
1 (0/1/0) |
NO
|
NO
|
MARK3 Chr14:103002170 |
|
Exonic |
MARK3
|
1 (0/0/1) |
NO
|
NO
|
CUX2 2607G/C |
point mutation |
|
CUX2
|
1 (0/1/0) |
NO
|
NO
|
LEPR hcv518168 |
point mutation |
|
LEPR
|
1 (1/0/0) |
NO
|
NO
|
TPH1 5'flanking T-1721G |
point mutation |
5'flanking |
TPH1
|
1 (0/1/0) |
NO
|
NO
|
KLC1 Chr14:103193796 |
|
Exonic |
KLC1
|
1 (0/0/1) |
NO
|
NO
|
CUX2 277G/A |
point mutation |
|
CUX2
|
1 (0/1/0) |
NO
|
NO
|
LNX1 SNP A-1948953 |
point mutation |
|
LNX1
|
1 (1/0/0) |
NO
|
NO
|
KLC1 Chr14:103193859 |
|
Exonic |
KLC1
|
1 (0/0/1) |
NO
|
NO
|
CUX2 3732T/C |
point mutation |
|
CUX2
|
1 (0/1/0) |
NO
|
NO
|
LOC100507206 1634tet |
microsatellite |
|
LOC100507206
|
1 (1/0/0) |
NO
|
NO
|
TDRD9 Chr14:103464808 |
|
Exonic |
TDRD9
|
1 (0/0/1) |
NO
|
NO
|
D18S453 |
microsatellite |
18p11.2 |
|
1 (1/0/0) |
YES
|
NO
|
LOC100507206 29818-insT |
point mutation |
|
LOC100507206
|
1 (1/0/0) |
NO
|
NO
|
TPH1 promoter 218A/C |
point mutation |
promoter |
TPH1
|
1 (0/1/0) |
NO
|
NO
|
TDRD9 Chr14:103576402 |
|
Exonic |
TDRD9
|
1 (0/0/1) |
NO
|
NO
|
D1 EcoR1 |
SNP |
|
DRD1
|
1 (0/1/0) |
NO
|
NO
|
LOC100507206 307CA1 |
microsatellite |
|
LOC100507206
|
1 (1/0/0) |
NO
|
NO
|
TPH2 C2755A |
point mutation |
|
TPH2
|
1 (1/0/0) |
NO
|
NO
|
BRF1 Chr14:104763646 |
|
Exonic |
BRF1
|
1 (0/0/1) |
NO
|
NO
|
D1S243 |
microsatellite |
|
PRKCZ
|
1 (1/0/0) |
NO
|
NO
|
LOC100507206 307CA2 |
microsatellite |
|
LOC100507206
|
1 (1/0/0) |
NO
|
NO
|
TPH2 promoter 703G/T |
point mutation |
promoter |
TPH2
|
1 (0/1/0) |
NO
|
NO
|
PACS2 Chr14:104904668 |
|
Exonic |
PACS2
|
1 (0/0/1) |
NO
|
NO
|
D1 Taq1 |
SNP |
|
DRD1
|
1 (0/1/0) |
NO
|
NO
|
LOC100507206 307GT4 |
microsatellite |
|
LOC100507206
|
1 (1/0/0) |
NO
|
NO
|
TPH1 BfaI Polymorphism |
SNP |
|
TPH1
|
1 (0/1/0) |
NO
|
NO
|
MTA1 Chr14:105007547 |
|
Exonic, 3'UTR |
MTA1
|
1 (0/0/1) |
NO
|
NO
|
D21S1260 |
microsatellite |
21q22.3 |
|
1 (1/0/0) |
NO
|
NO
|
LOC100507206 D12S1634 |
microsatellite |
|
LOC100507206
|
1 (1/0/0) |
NO
|
NO
|
TRPM2 c.2363C>T |
point mutation |
exon15 |
TRPM2
|
1 (0/1/0) |
NO
|
NO
|
NDE1 Chr16:15785033 C/G |
missense |
Exon 7 |
NDE1
|
1 (0/1/0) |
YES
|
NO
|
D21s1411 |
microsatellite |
21q22.3 |
|
1 (0/1/0) |
NO
|
NO
|
LOC100507206 D12S2075 |
microsatellite |
|
LOC100507206
|
1 (1/0/0) |
NO
|
NO
|
TRPM2 c.2890+55A>G |
point mutation |
intron18 |
TRPM2
|
1 (0/1/0) |
NO
|
NO
|
NDE1 Chr16:15785118 C/T |
missense |
Exon 7 |
NDE1
|
1 (0/1/0) |
YES
|
NO
|
D21S171 |
microsatellite |
21q22.3 |
|
1 (1/0/0) |
NO
|
NO
|
LOC100507206 D12S307 |
microsatellite |
|
LOC100507206
|
1 (1/0/0) |
NO
|
NO
|
TRPM2 c.3205C>T |
point mutation |
exon20 |
TRPM2
|
1 (0/1/0) |
NO
|
NO
|
NDE1 Chr16:15785177 C/T |
missense |
Exon 7 |
NDE1
|
1 (1/0/0) |
YES
|
NO
|
D21S1897 |
microsatellite |
21q22.3 |
|
1 (0/1/0) |
NO
|
NO
|
LOC100507206 D12SDK1 |
microsatellite |
|
LOC100507206
|
1 (1/0/0) |
NO
|
NO
|
TRPM2 c.3246+68C>T |
point mutation |
intron20 |
TRPM2
|
1 (0/1/0) |
NO
|
NO
|
NOS1 Exon 1c A/G |
point mutation |
Exon 1c |
NOS1
|
1 (0/1/0) |
NO
|
NO
|
D21S1903 |
microsatellite |
21q22.3 |
|
1 (0/1/0) |
NO
|
NO
|
LOC100507206 pufu-in/del |
point mutation |
|
LOC100507206
|
1 (1/0/0) |
NO
|
NO
|
TSPO exon4 Ala147Thr |
point mutation |
exon4 |
TSPO
|
1 (0/1/0) |
NO
|
YES
|
NOS1 Exon 1f L/S |
|
Exon 1f |
NOS1
|
1 (0/1/0) |
NO
|
NO
|
D21S212 |
microsatellite |
21q22.3 |
|
1 (0/1/0) |
NO
|
NO
|
MAB21L1 CAG/CTG repeat |
microsatellite |
|
MAB21L1
|
1 (0/1/0) |
NO
|
NO
|
TSPO exon4 His162Arg |
point mutation |
exon4 |
TSPO
|
1 (0/1/0) |
NO
|
YES
|
NOS3 Intron 4 VNTR 4a/b |
VNTR |
Intron |
NOS3
|
1 (0/1/0) |
NO
|
NO
|
D21S266 |
microsatellite |
21q22.3 |
|
1 (0/1/0) |
NO
|
NO
|
MAOA 1-8 allele |
others |
|
MAOA
|
1 (0/1/0) |
NO
|
NO
|
TYR (GA)n - (CA)n |
duplication |
|
TYR
|
1 (0/1/0) |
NO
|
NO
|
MUC4 Chr3:195492191 C/A |
missense |
Exon |
MUC4
|
1 (0/1/0) |
NO
|
NO
|
D22S1169 |
microsatellite |
|
|
1 (1/0/0) |
YES
|
NO
|
MAOA A1609G |
point mutation |
|
MAOA
|
1 (0/1/0) |
YES
|
YES
|
uMAOA |
duplication |
promoter |
MAOA
|
1 (0/1/0) |
NO
|
YES
|
GDNF Chr5:37812784 T/A |
point mutation |
3'UTR |
GDNF
|
1 (0/1/0) |
NO
|
NO
|
D22S279 |
microsatellite |
|
|
1 (1/0/0) |
YES
|
NO
|
VAMP2 C 25610873 10 |
point mutation |
|
VAMP2
|
1 (1/0/0) |
NO
|
NO
|
GDNF Chr5:37812782 T/A |
point mutation |
3'UTR |
GDNF
|
1 (0/1/0) |
NO
|
NO
|
D22S922 |
microsatellite |
|
|
1 (0/1/0) |
YES
|
NO
|
MAOA exon 8 Fnu4HI Polymorphism |
SNP |
exon 8 |
MAOA
|
1 (0/1/0) |
NO
|
NO
|
WFS1 A134A |
point mutation |
exon4 |
WFS1
|
1 (0/1/0) |
NO
|
NO
|
GDNF Chr5:37814769 G/A |
point mutation |
3'UTR |
GDNF
|
1 (0/1/0) |
NO
|
NO
|
D2 Taq1 |
SNP |
|
DRD2
|
1 (0/1/0) |
NO
|
NO
|
MAOA exon 8 RFLP |
SNP |
|
MAOA
|
1 (0/1/0) |
NO
|
YES
|
WFS1 E737K |
point mutation |
exon8 |
WFS1
|
1 (0/1/0) |
NO
|
NO
|
CYTH4 Promoter (GTTT)n |
STR |
Promoter |
CYTH4
|
1 (1/0/0) |
NO
|
NO
|
D3 Msc1 |
SNP |
|
DRD3
|
1 (0/1/0) |
NO
|
NO
|
MAOA exon 8 VNTR |
VNTR |
|
MAOA
|
1 (0/1/0) |
NO
|
YES
|
WFS1 exon8 A1832G |
point mutation |
exon8 |
WFS1
|
1 (0/1/0) |
NO
|
NO
|
MAOA CA |
point mutation |
|
MAOA
|
1 (1/0/0) |
NO
|
NO
|
D5S392 |
microsatellite |
|
SLC6A3
|
1 (0/0/1) |
NO
|
NO
|
MAOA Fnu4HI Polymorphism |
SNP |
|
MAOA
|
1 (1/0/0) |
NO
|
NO
|
5-HT2C Cys/Ser |
point mutation |
|
HTR2C
|
1 (0/1/0) |
NO
|
NO
|
DAOA 3'UTR SNP12 |
point mutation |
3'UTR |
DAOA
|
1 (1/0/0) |
YES
|
NO
|
MAOA-Fnu |
point mutation |
|
MAOA
|
1 (0/1/0) |
NO
|
YES
|
COMT G1947A |
point mutation |
|
COMT
|
1 (0/1/0) |
NO
|
YES
|
DAOA M12 |
point mutation |
|
DAOA
|
1 (0/1/0) |
YES
|
NO
|
MAOA intron 1 VNTR |
VNTR |
intron 1 |
MAOA
|
1 (0/1/0) |
NO
|
NO
|
WFS1 I720V |
point mutation |
exon8 |
WFS1
|
1 (0/1/0) |
NO
|
NO
|
COMT C1886G |
point mutation |
|
COMT
|
1 (1/0/0) |
NO
|
YES
|
DAOA M23 |
point mutation |
|
DAOA
|
1 (1/0/0) |
YES
|
NO
|
MAOA intron 2 dinucleotide repeat |
duplication |
intron 2 |
MAOA
|
1 (0/1/0) |
NO
|
NO
|
WFS1 I823I |
point mutation |
exon8 |
WFS1
|
1 (0/1/0) |
NO
|
NO
|
DAOA M24 |
point mutation |
|
DAOA
|
1 (0/1/0) |
YES
|
NO
|
MAOA LPR |
VNTR |
|
MAOA
|
1 (0/1/0) |
YES
|
YES
|
WFS1 K811K |
point mutation |
exon8 |
WFS1
|
1 (0/1/0) |
NO
|
NO
|
DAOA z6:1117 |
point mutation |
|
DAOA
|
1 (0/1/0) |
NO
|
NO
|
WFS1 N500N |
point mutation |
exon8 |
WFS1
|
1 (0/1/0) |
NO
|
NO
|
DAO MDAAO4 |
point mutation |
|
DAO
|
1 (0/1/0) |
YES
|
NO
|
WFS1 R456H |
point mutation |
exon8 |
WFS1
|
1 (0/1/0) |
NO
|
NO
|
DAO MDAAO5 |
point mutation |
|
DAO
|
1 (0/1/0) |
YES
|
NO
|
WFS1 S855S |
point mutation |
exon8 |
WFS1
|
1 (0/1/0) |
NO
|
NO
|
DAO MDAAO6 |
point mutation |
|
DAO
|
1 (0/1/0) |
YES
|
NO
|
WFS1 SNP1023 |
point mutation |
|
WFS1
|
1 (0/1/0) |
NO
|
YES
|
WFS1 SNP1185 |
point mutation |
|
WFS1
|
1 (0/1/0) |
NO
|
YES
|
DAT E15+1812T/C |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
MAOB 1-12 allele |
others |
|
MAOB
|
1 (1/0/0) |
NO
|
NO
|
WFS1 SNP1645 |
point mutation |
|
WFS1
|
1 (0/1/0) |
NO
|
YES
|
DAT E15+274G/C |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
WFS1 SNP1832 |
point mutation |
|
WFS1
|
1 (0/1/0) |
NO
|
YES
|
DAT E15+352G/A |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
MCP-1 A-2518G |
point mutation |
|
CCL2
|
1 (0/1/0) |
NO
|
NO
|
WFS1 SNP2206 |
point mutation |
|
WFS1
|
1 (0/1/0) |
NO
|
YES
|
DAT I10+117G/A |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
MDR1 exon26 C3435T |
point mutation |
exon 26 |
ABCB1
|
1 (1/0/0) |
NO
|
NO
|
WFS1 SNP2565 |
point mutation |
|
WFS1
|
1 (0/1/0) |
NO
|
YES
|
DAT I6+96G/C |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
MED12 exon42 duplication |
duplication |
exon42 |
MED12
|
1 (0/1/0) |
YES
|
NO
|
WFS1 SNP684 |
point mutation |
|
WFS1
|
1 (1/0/0) |
NO
|
YES
|
DAT I9-21G/A |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
MMP3 1171 5A/6A |
insertion/deletion |
|
MMP3
|
1 (0/1/0) |
YES
|
NO
|
WFS1 SNP935 |
point mutation |
|
WFS1
|
1 (0/1/0) |
NO
|
YES
|
DAT P+214A/G |
point mutation |
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
mtDNA 12358A>G |
point mutation |
|
mtDNA
|
1 (1/0/0) |
NO
|
NO
|
WFS1 V395V |
point mutation |
exon8 |
WFS1
|
1 (0/1/0) |
NO
|
NO
|
mtDNA 3644T>C |
point mutation |
|
mtDNA
|
1 (1/0/0) |
NO
|
NO
|
WFS1 V503G |
point mutation |
exon8 |
WFS1
|
1 (0/1/0) |
NO
|
NO
|
DBH A304S |
point mutation |
|
DBH
|
1 (0/1/0) |
NO
|
NO
|
mtDNA 5460G>A |
point mutation |
|
mtDNA
|
1 (0/1/0) |
NO
|
NO
|
White PolyT |
microsatellite |
21q22.3 |
|
1 (0/1/0) |
NO
|
NO
|
uVNTR MAOA |
|
|
MAOA
|
1 (0/1/0) |
NO
|
NO
|
rs1137070 c.1460 C/T |
|
c.1460 in MAOA exon 14 |
MAOA
|
1 (1/0/0) |
NO
|
NO
|
mtDNA A9115G |
point mutation |
|
mtDNA
|
1 (0/1/0) |
NO
|
NO
|
YWHAH 5'UTR (GCCTGCA)n |
duplication |
5'UTR |
YWHAH
|
1 (1/0/0) |
NO
|
NO
|
MAOA-CA MAOA |
|
in intron 2 of MAOA |
MAOA
|
1 (1/0/0) |
NO
|
NO
|
DDC microsatellite polymorphisms |
microsatellite |
|
DDC
|
1 (0/1/0) |
NO
|
NO
|
ANK3 exon 48 P1489S |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
MAOA-VNTR MAOA |
|
in intron 1 of MAOA |
MAOA
|
1 (0/1/0) |
NO
|
NO
|
DISC1 1013 G>A |
point mutation |
|
DISC1
|
1 (0/0/1) |
NO
|
NO
|
mtDNA D-loop C195T |
point mutation |
|
mtDNA_D-loop
|
1 (1/0/0) |
NO
|
NO
|
ANK3 exon 48 T1861M |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
rs1799835 c.941 T/G |
|
c.941 in MAOA exon 8 |
MAOA
|
1 (0/1/0) |
NO
|
NO
|
DISC1 1253 G>A |
point mutation |
|
DISC1
|
1 (0/0/1) |
NO
|
NO
|
mtDNA D-loop G16300A |
point mutation |
|
mtDNA_D-loop
|
1 (1/0/0) |
NO
|
NO
|
ANK3 exon 48 E1926D |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
rs58575285 |
|
|
GRIK4
|
1 (1/0/0) |
NO
|
NO
|
DISC1 1700 G>A |
point mutation |
|
DISC1
|
1 (0/0/1) |
NO
|
NO
|
mtDNA D-loop T114C |
point mutation |
|
mtDNA_D-loop
|
1 (1/0/0) |
NO
|
NO
|
ANK3 exon 48 S2043N |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
rs66554220 |
|
|
HLA-G
|
1 (1/0/0) |
NO
|
NO
|
DISC1 -215(TG)8-13 |
others |
5' upstream |
DISC1
|
1 (0/1/0) |
NO
|
YES
|
mtDNA ND4L T10652C |
point mutation |
|
mtDNA_ND4L
|
1 (1/0/0) |
NO
|
YES
|
ANK3 exon 48 I2158T |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
rs458178 |
|
|
|
1 (0/1/0) |
NO
|
NO
|
DISC1 2261 C>G |
point mutation |
|
DISC1
|
1 (0/0/1) |
NO
|
NO
|
mtDNA T3394C |
point mutation |
|
mtDNA
|
1 (0/1/0) |
NO
|
NO
|
ANK3 exon 48 D2319N |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
rs3045444 |
|
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DISC1 2425 TCATdel |
insertion/deletion |
|
DISC1
|
1 (0/0/1) |
NO
|
NO
|
MTHFD G1958A |
point mutation |
|
MTHFD1
|
1 (1/0/0) |
YES
|
NO
|
ANK3 exon 48 F2375V |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
rs10064525 |
|
|
SLC6A3
|
1 (0/1/0) |
NO
|
NO
|
DISC1 627 C>G |
point mutation |
|
DISC1
|
1 (0/0/1) |
NO
|
NO
|
ANK3 exon 48 S2409P |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
rs2550240 |
|
|
MUC4
|
1 (0/1/0) |
NO
|
NO
|
DISC1 74 G>A |
point mutation |
|
DISC1
|
1 (0/0/1) |
NO
|
NO
|
ANK3 exon 48 N2643S |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
rs13232194 |
|
|
NAPEPLD
|
1 (0/1/0) |
NO
|
NO
|
DISC1 790 C>T |
point mutation |
|
DISC1
|
1 (0/0/1) |
NO
|
NO
|
MTR A2756G |
point mutation |
|
MTR
|
1 (1/0/0) |
YES
|
NO
|
ANK3 exon 48 R2719T |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DISC1 887 A>G |
point mutation |
|
DISC1
|
1 (0/0/1) |
NO
|
NO
|
NCAM1 2208T>G |
point mutation |
|
NCAM1
|
1 (0/1/0) |
NO
|
YES
|
ANK3 exon 48 G2845E |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DISC1 A844G |
point mutation |
|
DISC1
|
1 (0/1/0) |
YES
|
NO
|
NCAM1 2256 2257 insATGG |
point mutation |
|
NCAM1
|
1 (0/1/0) |
NO
|
YES
|
ANK3 exon 48 S2858L |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DISC1 C1460T |
point mutation |
|
DISC1
|
1 (0/1/0) |
YES
|
NO
|
NCAM1 I621G>T |
point mutation |
|
NCAM1
|
1 (0/1/0) |
NO
|
YES
|
ANK3 exon 48 Q3264K |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DISC1 exon2 Pro/Leu |
point mutation |
exon2 |
DISC1
|
1 (0/1/0) |
NO
|
NO
|
NCAM1 IVS0-49de IG |
point mutation |
|
NCAM1
|
1 (0/1/0) |
NO
|
YES
|
ANK3 exon 48 S3521G |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DISC1 G65049 |
microsatellite |
|
DISC1
|
1 (0/1/0) |
YES
|
NO
|
NCAM1 IVS4+80G>C |
point mutation |
|
NCAM1
|
1 (0/1/0) |
NO
|
YES
|
ANK3 exon 48 E3563G |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DISC1 IVS1+3 A>T |
point mutation |
|
DISC1
|
1 (0/0/1) |
NO
|
NO
|
NCAM1 IVS6+32T>C |
point mutation |
|
NCAM1
|
1 (1/0/0) |
NO
|
YES
|
ANK3 exon 48 S3697C |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DISC1 T11840C |
point mutation |
|
DISC1
|
1 (0/1/0) |
YES
|
NO
|
NCAM1 IVS7+155G>T |
point mutation |
|
NCAM1
|
1 (0/1/0) |
NO
|
YES
|
ANK3 exon 48 N3789S |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DISC1 T2163A |
point mutation |
|
DISC1
|
1 (0/1/0) |
YES
|
NO
|
NCOR2 GC34E20A |
duplication |
|
NCOR2
|
1 (0/1/0) |
NO
|
NO
|
ANK3 exon 48 K3942R |
point mutation |
exon 48 |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DOCK9 (AAGTA) indel |
insertion/deletion |
|
DOCK9
|
1 (1/0/0) |
NO
|
NO
|
NDUFV2 -1020G>T |
point mutation |
|
NDUFV2
|
1 (0/1/0) |
NO
|
NO
|
DRD2/ANKK1 Taq-IA |
point mutation |
|
DRD2
|
1 (0/1/0) |
NO
|
NO
|
DNAH14 Chr1:225586971 A/T |
Stoploss |
Chr1:225586971 |
DNAH14
|
1 (0/0/1) |
NO
|
NO
|
NDUFV2 -2694A>G |
point mutation |
|
NDUFV2
|
1 (1/0/0) |
NO
|
NO
|
ARV1 Chr1:231114915 A/T |
Missense |
Chr1:231114915 |
ARV1
|
1 (0/0/1) |
NO
|
NO
|
NDUFV2 -3041T>G |
point mutation |
|
NDUFV2
|
1 (1/0/0) |
NO
|
NO
|
SLK Chr10:105779646 C/T |
Missense |
Chr10:105779646 |
SLK
|
1 (0/0/1) |
NO
|
NO
|
DRD1 EcoRI Polymorphism |
SNP |
|
DRD1
|
1 (0/1/0) |
NO
|
NO
|
NDUFV2 -3245T>C |
point mutation |
|
NDUFV2
|
1 (1/0/0) |
NO
|
NO
|
CFAP46 Chr10:134730168 G/A |
Missense |
Chr10:134730168 |
CFAP46
|
1 (0/0/1) |
NO
|
NO
|
DRD1 RFLP |
SNP |
|
DRD1
|
1 (0/1/0) |
NO
|
NO
|
NDUFV2 -3542G>A |
point mutation |
|
NDUFV2
|
1 (1/0/0) |
NO
|
NO
|
CARD16 Chr11:104916205 A/G |
Upstream |
Chr11:104916205 |
CARD16
|
1 (0/0/1) |
NO
|
NO
|
DRD2 -141CIns/Del |
insertion/deletion |
|
DRD2
|
1 (0/1/0) |
NO
|
YES
|
ZPR1 Chr11:116652892 A/T |
Missense |
Chr11:116652892 |
ZNF259
|
1 (0/0/1) |
NO
|
NO
|
SLU7 Chr5:159840980 T/C |
Missense |
Chr5:159840980 |
SLU7
|
1 (0/0/1) |
NO
|
NO
|
DRD2 -151ins/del |
insertion/deletion |
|
DRD2
|
1 (0/1/0) |
NO
|
NO
|
WWC1 Chr5:167896045 G/A |
others |
Chr5:167896045 |
WWC1
|
1 (0/0/1) |
NO
|
NO
|
DRD2 5'flanking -141C Ins/Del |
insertion/deletion |
5'flanking |
DRD2
|
1 (0/1/0) |
YES
|
NO
|
SLC6A2 Gly478Ser |
point mutation |
|
SLC6A2
|
1 (0/1/0) |
YES
|
NO
|
TAB2 Chr6:149699617 G/A |
Missense |
Chr6:149699617 |
TAB2
|
1 (0/0/1) |
NO
|
NO
|
DRD2 (CA)n |
duplication |
|
DRD2
|
1 (0/1/0) |
NO
|
NO
|
SLC6A2 TaqI polymorphism |
SNP |
|
SLC6A2
|
1 (0/1/0) |
NO
|
NO
|
MTOR Chr1:11194520 C/T |
Splicing |
Chr1:11194520 |
MTOR
|
1 (0/0/1) |
NO
|
NO
|
DRD2 intron 1 (TG)n |
duplication |
intron1 |
DRD2
|
1 (0/1/0) |
NO
|
NO
|
SLC6A2 Thr99Ile |
point mutation |
|
SLC6A2
|
1 (0/1/0) |
YES
|
NO
|
CASP1 Chr11:104901923 |
Nonframeshift del |
Chr11:104901923 |
CASP1
|
1 (0/0/1) |
NO
|
NO
|
DRD2 microsatellite |
microsatellite |
|
DRD2
|
1 (1/0/0) |
NO
|
YES
|
SLC6A2 Val245Ile |
point mutation |
|
SLC6A2
|
1 (0/1/0) |
YES
|
NO
|
SLC25A21 Chr14:37147560 C/T |
others |
Chr14:37147560 |
SLC25A21
|
1 (0/0/1) |
NO
|
NO
|
DRD2 polymorphism |
others |
|
DRD2
|
1 (0/1/0) |
NO
|
NO
|
SLC6A2 Val449Ile |
point mutation |
|
SLC6A2
|
1 (0/1/0) |
YES
|
NO
|
ID1 Chr20:30193296 T/G |
Missense |
Chr20:30193296 |
ID1
|
1 (0/0/1) |
NO
|
NO
|
SLC6A2 Val69Ile |
point mutation |
|
SLC6A2
|
1 (0/1/0) |
YES
|
NO
|
CDV3 Chr3:133305557 A/T |
Missense |
Chr3:133305557 |
CDV3
|
1 (0/0/1) |
NO
|
NO
|
PITPNM2 GC18E01A |
point mutation |
|
PITPNM2
|
1 (0/1/0) |
NO
|
NO
|
ODZ2 Chr5:167627125 C/T |
Missense |
Chr5:167627125 |
TENM2
|
1 (0/0/1) |
NO
|
NO
|
RTN4 3'UTR CAA insertion |
insertion/deletion |
3'UTR |
RTN4
|
1 (0/1/0) |
YES
|
NO
|
GRN C/T |
point mutation |
|
GRN
|
1 (1/0/0) |
YES
|
NO
|
NOS1 exon13 SNP2 |
point mutation |
exon13 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
NOV Chr8:120430415 G/A |
missense point mutation |
Chr8:120430415 |
NOV
|
1 (0/0/1) |
NO
|
NO
|
DRD2 (TG)n |
duplication |
|
DRD2
|
1 (1/0/0) |
NO
|
NO
|
NOS1 exon15 IVS15+38C/T |
point mutation |
exon15 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
INSL6 Chr9:5164252 C/T |
missense point mutation |
Chr9:5164252 |
INSL6
|
1 (0/0/1) |
NO
|
NO
|
DRD3 allele1/allele2 |
others |
|
DRD3
|
1 (0/1/0) |
NO
|
NO
|
NOS1 exon16 2607C/T |
point mutation |
exon16 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
LOC285033 Chr2:96907615 A/C |
missense point mutation |
Chr2:96907615 |
LOC285033
|
1 (0/0/1) |
NO
|
NO
|
NOS1 exon17 2712C/T |
point mutation |
exon17 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
NCEH1 Chr3:172365793 C/T |
missense point mutation |
Chr3:172365793 |
NCEH1
|
1 (0/0/1) |
NO
|
NO
|
DRD3 exon1 D3 polymorphism |
others |
exon1 |
DRD3
|
1 (0/1/0) |
NO
|
NO
|
NOS1 exon17 IVS17+15A/G |
point mutation |
exon17 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
ZAN Chr7:100382373 C/T |
point mutation |
Chr7:100382373 |
ZAN
|
1 (0/0/1) |
NO
|
NO
|
NOS1 exon18 SNP3 |
point mutation |
exon18 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
FAM38B Chr18:10759858 T/C |
point mutation |
Chr18:10759858 |
PIEZO2
|
1 (0/0/1) |
NO
|
NO
|
DRD4 2-10 allele |
others |
|
DRD4
|
1 (0/1/0) |
NO
|
YES
|
NOS1 exon19 IVS19+13T/G |
point mutation |
exon19 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
FAM83F rs3021268 |
single nucleotide variation |
rs3021268 doesn't map to any assembly. |
FAM83F
|
1 (0/1/0) |
NO
|
NO
|
DRD4 48bp repeat |
duplication |
|
DRD4
|
1 (0/1/0) |
NO
|
NO
|
NOS1 exon20 137244A/G |
point mutation |
exon20 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
ANK3 Chr10:61786761 A/G |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
NOS1 exon21 3258C/T |
point mutation |
exon21 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
ANK3 Chr10:61787065 TA/- |
insertion/deletion |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
NOS1 exon27 4063G/A |
point mutation |
exon27 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
ANK3 Chr10:61788626 G/T |
point mutation |
3'UTR |
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DRD4 HincII Polymorphism |
SNP |
|
DRD4
|
1 (0/1/0) |
NO
|
NO
|
NOS1 exon27 4065G/A |
point mutation |
exon27 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
ANK3 Chr10:61789498 AC/- |
insertion/deletion |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DRD5 (CT/GT/GA)n |
duplication |
|
DRD5
|
1 (0/1/0) |
NO
|
NO
|
NOS1 exon27 4154G/A |
point mutation |
exon27 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
ANK3 Chr10:61789512 C/- |
insertion/deletion |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DRD5 D4S615 |
microsatellite |
|
DRD5
|
1 (0/1/0) |
YES
|
YES
|
NOS1 exon27 IVS27+14T/G |
point mutation |
exon27 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
ANK3 Chr10:61789556 C/- |
insertion/deletion |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
G'>DRP2 5'-flanking -975C>G |
point mutation |
5'flanking |
DRP2
|
1 (0/1/0) |
NO
|
NO
|
NOS1 exon27 IVS27+9C/A |
point mutation |
exon27 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
ANK3 Chr10:61819783 T/G |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DRP2 exon13 1506T>C |
point mutation |
exon13 |
DRP2
|
1 (0/1/0) |
NO
|
NO
|
NOS1 exon27 SNP5 |
point mutation |
exon27 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
ANK3 Chr10:61841574 T/- |
insertion/deletion |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DRP2 exon14 *2236T>C |
point mutation |
exon14 |
DRP2
|
1 (0/1/0) |
NO
|
NO
|
NOS1 exon29 SNP4 |
point mutation |
exon29 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
ANK3 Chr10:61843365 C/G |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DRP2 exon4 352G>A |
point mutation |
exon4 |
DRP2
|
1 (0/1/0) |
NO
|
NO
|
NOS1 exon7 IVS7-15C/G |
point mutation |
exon7 |
NOS1
|
1 (0/0/1) |
YES
|
NO
|
ANK3 Chr10:61900256 G/A |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DRP2 exon4 426C>T |
point mutation |
exon4 |
DRP2
|
1 (0/1/0) |
NO
|
NO
|
ANK3 Chr10:61900727 G/C |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DUSP6 exon1 Leu111Val |
point mutation |
exon1 |
DUSP6
|
1 (0/1/0) |
NO
|
YES
|
NOS1 SNP1 |
point mutation |
|
NOS1
|
1 (0/1/0) |
YES
|
NO
|
ANK3 Chr10:61900857 G/A |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
DUSP6 Leu114Val |
point mutation |
|
DUSP6
|
1 (0/1/0) |
NO
|
YES
|
NOS3 G894T |
point mutation |
|
NOS3
|
1 (0/1/0) |
NO
|
YES
|
ANK3 Chr10:61901317 -/TG |
insertion/deletion |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
ERBB4 SNV7 G>A |
point mutation |
|
ERBB4
|
1 (1/0/0) |
NO
|
NO
|
NOS3 Intron4 VNTR |
VNTR |
Intron4 |
NOS3
|
1 (0/1/0) |
NO
|
YES
|
ANK3 Chr10:61901321 T/G |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
ERBB4 SNV8 A insertion/deletion |
insertion/deletion |
|
ERBB4
|
1 (0/1/0) |
NO
|
NO
|
NOS3 T-786C |
point mutation |
|
NOS3
|
1 (0/1/0) |
NO
|
YES
|
ANK3 Chr10:61941143 C/G |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
ERDA1 CAG/CTG repeat |
microsatellite |
|
ERDA1
|
1 (0/1/0) |
NO
|
NO
|
ANK3 Chr10:61958307 G/T |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
NOTCH4 promoter A>G |
point mutation |
promoter |
NOTCH4
|
1 (0/1/0) |
NO
|
NO
|
ANK3 Chr10:62149642 C/T |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
FEZ1 IVS3+2509C>T |
point mutation |
|
FEZ1
|
1 (0/1/0) |
YES
|
NO
|
NQO1 C609T |
point mutation |
|
NQO1
|
1 (0/1/0) |
NO
|
YES
|
ANK3 Chr10:62150190 G/A |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
FEZ1 IVS4+1077T>C |
point mutation |
|
FEZ1
|
1 (0/1/0) |
YES
|
NO
|
NR2E1 g. -1429 |
point mutation |
|
NR2E1
|
1 (0/1/0) |
YES
|
NO
|
ANK3 Chr10:62332894 -/A |
insertion/deletion |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
FEZ1 IVS9+66A>T |
point mutation |
|
FEZ1
|
1 (0/1/0) |
YES
|
NO
|
ANK3 Chr10:62332895 A/AA |
duplication |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
FLJ11021 GC6E04A |
point mutation |
|
RSRC2
|
1 (0/1/0) |
NO
|
NO
|
ANK3 Chr10:62332985 T/- |
insertion/deletion |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
FLJ22471 GC32E03A |
point mutation |
|
CCDC92
|
1 (0/1/0) |
NO
|
NO
|
NRG1 D8S1810 |
microsatellite |
|
NRG1
|
1 (1/0/0) |
NO
|
NO
|
ANK3 Chr10:62333120 ACCAACCA/- |
insertion/deletion |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
FLJ22471 GC32E04A |
point mutation |
|
CCDC92
|
1 (1/0/0) |
NO
|
NO
|
NRG1 exon 11 Val>Leu |
point mutation |
exon 11 |
|
1 (0/1/0) |
YES
|
NO
|
ANK3 Chr10:62493812 G/C |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
GABRA1 -181A/G |
point mutation |
|
GABRA1
|
1 (0/1/0) |
NO
|
YES
|
NRG1 SNP88NR221533 |
point mutation |
|
NRG1
|
1 (0/1/0) |
NO
|
NO
|
ANK3 Chr10:62494029 A/G |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
GABRA1 -471T/C |
point mutation |
|
GABRA1
|
1 (0/1/0) |
NO
|
YES
|
NRG1 SNP8NRG221132 |
point mutation |
|
NRG1
|
1 (0/1/0) |
YES
|
NO
|
ANK3 Chr10:62494113 C/T |
point mutation |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
GABRA1 IVS2-712(GT)n |
microsatellite |
|
GABRA1
|
1 (1/0/0) |
NO
|
YES
|
ANK3 Chr10:62494201 CT/CTATATTAT |
insertion/deletion |
|
ANK3
|
1 (0/1/0) |
NO
|
NO
|
GABRA1 IVS9+76A/G |
point mutation |
|
GABRA1
|
1 (0/1/0) |
NO
|
YES
|
CACNA1C Chr12:2161733 G/C |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GABRA3 (AC)n |
duplication |
|
GABRA3
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2161930 C/T |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GABRA3 CA repeat |
microsatellite |
|
GABRA3
|
1 (1/0/0) |
NO
|
NO
|
NTS 166C>G |
point mutation |
|
NTS
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2161934 G/A |
point mutation |
Promoter |
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GABRA3 GDB156286 |
VNTR |
|
GABRA3
|
1 (0/1/0) |
NO
|
NO
|
NTS 3A>G |
point mutation |
|
NTS
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2161984 C/A |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GABRA5 +11547 (CA)n |
microsatellite |
|
GABRA5
|
1 (0/1/0) |
NO
|
NO
|
P2RX7 NBG6 |
microsatellite |
|
P2RX7
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2162059 -/GGGG/CGGG/AGGG |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GABRA5 3'UTR 1-8 allele |
others |
|
GABRA5
|
1 (1/0/0) |
NO
|
YES
|
P2RX7 P2RX73 |
duplication |
|
P2RX7
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2162201 -/CGGCG |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GABRA5 (CA)n |
polymorphic dinucleotide repeat marker |
|
GABRA5
|
1 (1/0/0) |
NO
|
YES
|
PCNT2-AluI |
microsatellite |
21q22.3 |
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2162217 G/A |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GABRA5 GDB162554 |
VNTR |
|
GABRA5
|
1 (1/0/0) |
NO
|
NO
|
PENK polymorphisms |
VNTR |
|
PENK
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2272007 C/T |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GABRb1 (GATA)n |
tetranucleotide repeat |
|
GABRB1
|
1 (1/0/0) |
NO
|
NO
|
PER2 2087A/G |
point mutation |
|
PER2
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2284208 -/TGTTCAAACCTGTGT |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GABRB3 (CA) repeat |
microsatellite |
|
GABRB3
|
1 (0/1/0) |
NO
|
NO
|
PER2 2114G/A |
point mutation |
|
PER2
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2286800 -/TCTTTCTT |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GABRB3 GDB160763 |
VNTR |
|
GABRB3
|
1 (0/1/0) |
NO
|
NO
|
PER2 2117G/A |
point mutation |
|
PER2
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2286819 -/TT |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GCH1 -959G/A |
point mutation |
|
GCH1
|
1 (1/0/0) |
NO
|
NO
|
PFKL |
microsatellite |
21q22.3 |
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2286820 -/T |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GCLC 5'UTR repeat |
microsatellite |
5'UTR |
GCLC
|
1 (0/1/0) |
NO
|
NO
|
PIK3C3 -432C->T |
point mutation |
|
PIK3C3
|
1 (1/0/0) |
YES
|
NO
|
CACNA1C Chr12:2291321 -/AT |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GNAL intron10 T/G |
point mutation |
intron10 |
GNAL
|
1 (0/1/0) |
NO
|
NO
|
PIK3C3 promoter -86insC |
insertion/deletion |
promoter |
PIK3C3
|
1 (0/0/1) |
YES
|
NO
|
CACNA1C Chr12:2292413 -/A |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GNAL intron3 A/G |
point mutation |
intron 3 |
GNAL
|
1 (0/1/0) |
NO
|
NO
|
PIK4CA -31(A>G) |
point mutation |
|
PI4KA
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2292742 -/C |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GNAZ exon2 309C/T |
SNP |
exon2 |
GNAZ
|
1 (1/0/0) |
NO
|
NO
|
PIK4CA E2079Q |
point mutation |
|
PI4KA
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2296694 -/T |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GNB3 C825T |
point mutation |
|
GNB3
|
1 (0/1/0) |
YES
|
YES
|
PIK4CA R2259C |
point mutation |
|
PI4KA
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2296695 GG/TGG |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
PIP5K2A -1007C>T |
point mutation |
|
PIP4K2A
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2297340 -/CT |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRIN1 exon6 19700A/G |
point mutation |
exon6 |
GRIN1
|
1 (0/1/0) |
NO
|
NO
|
PIP5K2A Exon10 1257T->G |
point mutation |
exon10 |
PIP4K2A
|
1 (0/0/1) |
NO
|
NO
|
CACNA1C Chr12:2297530 -/CT |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRIN1 intron11 6608A/G |
point mutation |
intron11 |
GRIN1
|
1 (1/0/0) |
NO
|
NO
|
PIP5K2A Exon10 1412G->C |
point mutation |
exon 0 |
PIP4K2A
|
1 (0/0/1) |
NO
|
NO
|
CACNA1C Chr12:2300919 -/CA |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRIN1 promoter 1001G/C |
point mutation |
promoter |
GRIN1
|
1 (1/0/0) |
NO
|
NO
|
PIP5K2A Exon10 Codon 391(GAA->GAG) |
point mutation |
exon10_codon391 |
PIP4K2A
|
1 (0/0/1) |
NO
|
NO
|
CACNA1C Chr12:2300934 -/CTCCACAGGCACAT |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRIN2A promoter (GT)n |
microsatellite |
promoter |
GRIN2A
|
1 (1/0/0) |
NO
|
NO
|
PIP5K2A Exon5 Codon 199(GTA->GTG) |
point mutation |
exon5_codon199 |
PIP4K2A
|
1 (0/0/1) |
NO
|
NO
|
CACNA1C Chr12:2301013 -/CACT |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
PIP5K2A Exon7 N251S |
point mutation |
exon7 |
PIP4K2A
|
1 (0/0/1) |
NO
|
NO
|
CACNA1C Chr12:2301016 -/T |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRIN2B 366C/G |
point mutation |
|
GRIN2B
|
1 (0/1/0) |
NO
|
NO
|
PIP5K2A Exon8 Codon 309(CCG->CCA) |
point mutation |
exon8_codon309 |
PIP4K2A
|
1 (0/0/1) |
NO
|
NO
|
CACNA1C Chr12:2301048 -/G |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRIN2B A5806C |
point mutation |
|
GRIN2B
|
1 (1/0/0) |
YES
|
NO
|
PIP5K2A Exon8 IVS8+20C->G |
point mutation |
exon 8 |
PIP4K2A
|
1 (0/0/1) |
NO
|
NO
|
CACNA1C Chr12:2301049 -/T |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRIN2B T5988C |
point mutation |
|
GRIN2B
|
1 (1/0/0) |
YES
|
NO
|
PIP5K2A Exon9 Intron 9 CT repeat |
microsatellite |
exon 9_intron9 |
PIP4K2A
|
1 (1/0/0) |
YES
|
NO
|
CACNA1C Chr12:2301051 -/C |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 129964 SNP37 |
point mutation |
|
ADRBK2
|
1 (0/1/0) |
NO
|
NO
|
PKNOX1 |
microsatellite |
21q22.3 |
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2301188 -/ATAC/ACAC |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 14087 SNP23 |
point mutation |
|
ADRBK2
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2302620 -/A |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 14454 SNP24 |
point mutation |
|
ADRBK2
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2302621 -/A/AA |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 15401 SNP28 |
point mutation |
|
ADRBK2
|
1 (1/0/0) |
NO
|
NO
|
PLA2G10 (AAT)n |
microsatellite |
|
PLA2G10
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2308364 -/GG |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 15667 SNP29 |
point mutation |
|
ADRBK2
|
1 (0/1/0) |
NO
|
NO
|
PLCG1 exon26 C/T |
point mutation |
exon26 |
PLCG1
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2308644 -/C |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 20256 SNP32 |
point mutation |
|
ADRBK2
|
1 (0/1/0) |
NO
|
NO
|
PLCG1 exon31 G/T |
point mutation |
exon31 |
PLCG1
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2314099 AAAGTATAA/- |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 2992 SNP14 |
point mutation |
|
ADRBK2
|
1 (0/1/0) |
NO
|
NO
|
PLCG1 exon9 A/G |
point mutation |
exon9 |
PLCG1
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2314103 -/A |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 600 SNP12 |
point mutation |
|
ADRBK2
|
1 (0/1/0) |
NO
|
NO
|
PON1 L55M |
point mutation |
|
PON1
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2317001 -/AA/AAA |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 9046 SNP19 |
point mutation |
|
ADRBK2
|
1 (0/1/0) |
NO
|
NO
|
PON1 Q192R |
point mutation |
|
PON1
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2317010 A/C |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 P-1 |
point mutation |
|
ADRBK2
|
1 (1/0/0) |
NO
|
NO
|
PPP2R2C Intron1d 99-24169/139 |
point mutation |
Intron1d |
PPP2R2C
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2317010 AC/CC |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 P-2 |
point mutation |
|
ADRBK2
|
1 (0/1/0) |
NO
|
NO
|
PPP2R2C Intron4 24-247/216 |
point mutation |
Intron4 |
PPP2R2C
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2321310 -/C |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 P-5 |
point mutation |
|
ADRBK2
|
1 (1/0/0) |
NO
|
NO
|
PPP2R2C Intron5 24-257/320 |
point mutation |
Intron5 |
PPP2R2C
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2323140 -/T |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 P-6 |
point mutation |
|
ADRBK2
|
1 (1/0/0) |
NO
|
NO
|
PPP2R2C Intron5 99-24175/218 |
point mutation |
Intron5 |
PPP2R2C
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2323807 A/C |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRK3 SNP36 |
point mutation |
|
ADRBK2
|
1 (0/1/0) |
NO
|
NO
|
PPP3CC-CC33 |
point mutation |
|
PPP3CC
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2328828 A/T |
point mutation |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRM3 +1131C/T |
point mutation |
|
GRM3
|
1 (0/1/0) |
YES
|
NO
|
PPP3CC-CCS3 |
point mutation |
|
PPP3CC
|
1 (1/0/0) |
NO
|
NO
|
CACNA1C Chr12:2329069 G/T |
point mutation |
intron |
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GRM7 hcv11751218 |
point mutation |
|
GRM7
|
1 (1/0/0) |
NO
|
NO
|
PRKCZ(AC)24 |
microsatellite |
|
PRKCZ
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2332571 T/- |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
PRKCZ(CA)13 |
microsatellite |
|
PRKCZ
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2334223 -/G |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
PRKCZ(GT)17 |
microsatellite |
|
PRKCZ
|
1 (0/1/0) |
NO
|
NO
|
CACNA1C Chr12:2335287 -/CG |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GSTM1 positive/null |
insertion/deletion |
|
GSTM1
|
1 (1/0/0) |
NO
|
NO
|
PRODH-1482 |
point mutation |
|
PRODH
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2335288 -/CG/CGCG |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
GSTT1 positive/null |
insertion/deletion |
|
GSTT1
|
1 (0/1/0) |
NO
|
NO
|
PRODH-1945 |
point mutation |
|
PRODH
|
1 (0/1/0) |
YES
|
NO
|
CACNA1C Chr12:2335298 -/A/C |
insertion/deletion |
|
CACNA1C
|
1 (0/1/0) |
NO
|
NO
|
16p11.2 microduplications |
duplication |
|
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35441380 G/C |
|
Chr11:35441380 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35441311 G/A |
|
Chr11:35441311 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
MAOA microsatellite polymorphisms |
microsatellite |
|
MAOA
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35441254 C/T |
|
Chr11:35441254 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35440927 A/G |
|
Chr11:35440927 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35440635 G/A |
|
Chr11:35440635 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35440563 C/G |
|
Chr11:35440563 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35440498 G/A |
|
Chr11:35440498 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35344202 G/T |
|
Chr11:35344202 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35344107 G/A |
|
Chr11:35344107 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35339061 C/T |
|
Chr11:35339061 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35338989 G/A |
|
Chr11:35338989 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35282452 C/T |
|
Chr11:35282452 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35280227 C/T |
|
Chr11:35280227 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35279202 A/G |
|
Chr11:35279202 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|
SLC1A2 Chr11:35276479 C/T |
|
Chr11:35276479 |
SLC1A2
|
0 (0/0/0) |
NO
|
NO
|