SNP Report

Basic Info

Name	rs41311993 dbSNP Ensembl
Location	chr1:23875221 - 23875221(1)
Variant Alleles	G/T
Ancestral Allele	G
Minor Allele	T
Minor Allele Frequence	0.00259585
Functional Annotation	missense_variant. Polyphen Annotation: possibly damaging(ENST00000374472) SIFT Annotation: tolerated(ENST00000374472)
Consequence to Transcript	missense_variant(ENST00000374472)
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
Minocci, D.,2011	524C>A		Fisher's Exact test: allele, OR (95%C.I.)=4.74 (2.30-9.78), ...... Fisher's Exact test: allele, OR (95%C.I.)=4.74 (2.30-9.78), P-value = 0.001 More...	Significant association was found . Significant association was found .	Positive

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 rs41311993 (count: 0) View in gBrowse (chr1:23875221..23875221 )

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

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