SNP Report

Basic Info
Name rs4627791 dbSNP Ensembl
Location chr3:32306332 - 32306332(1)
Variant Alleles A/G
Ancestral Allele A
Minor Allele G
Minor Allele Frequence 0.236621
Functional Annotation intron_variant.
Consequence to Transcript intron_variant(ENST00000307526, ENST00000458535)
No. of Studies 1 (Positive: 0; Negative: 0; Trend: 1)
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
Jiang, Y.,2011 Non-weighted test under H0: P-value(additive)=0.00000238, P-...... Non-weighted test under H0: P-value(additive)=0.00000238, P-value(dominant)=0.00000773, P-value(recessive)=0.0035; weighted test under H'0: P-value(additive)=0.00000634, P-value(dominant)=0.0000159, P-value(recessive)=0.00191; logistic regression: P-value(additive)=0.0000046, P-value(dominant)=0.0000218, P-value(recessive)=0.00284 More... Suggestive association was found. Suggestive association was found. Trend

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
CMTM8 CKLF-like MARVEL transmembrane domain containing 8 3p22.2 2(1/1/0)

SNPs in LD with rs4627791 (count: 0) View in gBrowse (chr3:32306332..32306332 )

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

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