SNP Report

Basic Info
Name rs2501432 dbSNP Ensembl
Location chr1:23875430 - 23875430(1)
Variant Alleles T/C
Ancestral Allele C
Minor Allele T
Minor Allele Frequence 0.346645
Functional Annotation missense_variant.
Polyphen Annotation: benign(ENST00000374472)
SIFT Annotation: tolerated(ENST00000374472)
Consequence to Transcript missense_variant(ENST00000374472)
No. of Studies 1 (Positive: 0; Negative: 1; 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
Minocci, D.,2011 315A>G Fisher's Exact test: allele, OR (95%C.I.)=0.80 (0.46-1.41), ...... Fisher's Exact test: allele, OR (95%C.I.)=0.80 (0.46-1.41), P-value = 0.15 More... No significant association was observed. No significant association was observed. Negative

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
CNR2 cannabinoid receptor 2 (macrophage) 1p 1(1/0/0)

SNPs in LD with rs2501432 (count: 0) View in gBrowse (chr1:23875430..23875430 )

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

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