SNP Report

Basic Info
Name |
rs1414686
dbSNP
Ensembl
|
Location |
chr10:54651899 - 54651899(1) |
Variant Alleles |
T/C |
Ancestral Allele |
T |
Minor Allele |
C |
Minor Allele Frequence |
0.0848642 |
Functional Annotation |
intron_variant; NMD_transcript_variant; non_coding_transcript_variant.
|
Consequence to Transcript |
intron_variant(ENST00000320301, ENST00000361849, ENST00000373955, ENST00000373956, ENST00000373957, ENST00000373965, ENST00000395430, ENST00000395432, ENST00000395433, ENST00000395438, ENST00000395440, ENST00000395442, ENST00000395445, ENST00000395446, ENST00000409834, ENST00000414367, ENST00000414778, ENST00000422842, ENST00000437009, ENST00000448885, ENST00000458638, ENST00000495484, ENST00000612394, ENST00000613346, ENST00000613657, ENST00000614895, ENST00000616114, ENST00000617051, ENST00000617271, ENST00000621708, ENST00000622048); NMD_transcript_variant(ENST00000373956, ENST00000414367, ENST00000448885); non_coding_transcript_variant(ENST00000422842) |
No. of Studies |
1 (Positive: 1; Negative: 0; Trend: 0) |
Source |
Literature |
Overlap with SZ? |
NO
|
Overlap with MDD? |
NO
|

SNP related studies (count: 1)

SNP related genes (count: 1)
The LD data used here is based on HapMap rel#27. LD SNP pairs were selected with a threshold r2<=0.8.
Literature-origin SNPs (count: 0)
LD-proxies (count: 6)

rs_ID |
Literature-origin SNPs with LD |
Functional Annotation |
r2[population] |
rs11004434
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
0.805[CHB]
|
rs1414688
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
0.857[CHD]
|
rs10509016
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
1.0[CHB]; 1.0[CHD]; 1.0[JPT]
|
rs12257633
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
1.0[CHB]; 0.863[JPT]
|
rs11004433
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
0.863[CHB]
|
rs1414687
|
|
intron_variant; NMD_transcript_variant; non_coding_transcript_variant |
1.0[CHB]; 1.0[CHD]; 1.0[JPT]
|

Overlap with SZ from cross-disorder studies (count: 0)

Overlap with MDD from cross-disorder studies (count: 0)