BDgene

SNP Report

Basic Info
Name rs713770 dbSNP Ensembl
Location chr22:35271982 - 35271982(1)
Variant Alleles A/G
Ancestral Allele A
Minor Allele G
Minor Allele Frequence 0.453674
Functional Annotation intron_variant; NMD_transcript_variant.
Consequence to Transcript intron_variant(ENST00000216106, ENST00000418170); NMD_transcript_variant(ENST00000418170)
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)
Reference Allele Change Risk Allele Statistical Values Author Comments Result Category
Potash, J. B., 2008 A/G Family-based P-value = 0.049 for all BPAD subjects, family-b...... Family-based P-value = 0.049 for all BPAD subjects, family-based P-value = 0.018 for BPAD subjects with psychotic symptoms, family-based P-value = 0.047 (3-marker sliding window with indicated marker first of the three), family-based P-value = 0.015 (3-marker sliding window with indicated marker first of the three using only those BPAD subjects with psychotic symptoms).Case-control P-value = 0.17 for all BPAD subjects, case-control P-value = 0.19 for BPAD subjects with psychotic symptoms, case-control P-value = 0.17 (3-marker sliding window with indicated marker first of the three), case-control P-value = 0.18 (3-marker sliding window with indicated marker first of the three using only those BPAD subjects with psychotic symptoms). More... The strongest signal in the family-based analysis emerged fr...... The strongest signal in the family-based analysis emerged from the 11 SNP HMG2L1/TOM1 haploblock. More... Positive

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
HMGXB4 HMG box domain containing 4 22q13 1(1/0/0)

SNPs in LD with rs713770 (count: 52) View in gBrowse (chr22:35244950..35316184 )
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: 52)


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

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