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)