SNP Report

Basic Info
Name rs4963954 dbSNP Ensembl
Location chr12:26113698 - 26113698(1)
Variant Alleles C/T
Ancestral Allele T
Minor Allele C
Minor Allele Frequence 0.351837
No. of Studies 1 (Positive: 1; Negative: 0; Trend: 0)
Source Literature
Overlap with SZ? NO
Overlap with MDD? YES

SNP related studies (count: 1)
Reference Allele Change Risk Allele Statistical Values Author Comments Result Category
Soria, V.,2010 X2-tests: allele P-value = 0.035, Model Dominant,...... X2-tests: allele P-value = 0.035, Model Dominant, genotype P-value = 0.019, OR(95%CI)=0.66 (0.47-0.93) More... Significant association was found in BD. Significant association was found in BD. Positive

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
BHLHE41 basic helix-loop-helix family, member e41 12p12.1 3(2/1/0)

SNPs in LD with rs4963954 (count: 2) View in gBrowse (chr12:26113698..26119891 )
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: 2)

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

Overlap with MDD from cross-disorder studies (count: 1)
Reference Statistical Result Description Result Category
Soria, V.,2010 X2-tests:allele P-value > 0.05, genotype P-value > 0.05 in all model No significant association was observed. Negative