SNP Report

Basic Info

Name	rs113270504 dbSNP Ensembl
Location	chr8:37835186 - 37835186(1)
Variant Alleles	G/A/C
Ancestral Allele	G
Minor Allele	A
Minor Allele Frequence	0.00638978
Functional Annotation	intron_variant; missense_variant. Polyphen Annotation: benign(ENST00000412232) SIFT Annotation: deleterious(ENST00000412232)
Consequence to Transcript	intron_variant(ENST00000315215); missense_variant(ENST00000412232)
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
Georgi, B., 2014	G/A		13 in BPI, 9 in Well 13 in BPI, 9 in Well	Top 30 Amish-specific putative damaging exonic missense vari...... Top 30 Amish-specific putative damaging exonic missense variants by prevalence in affected individuals. More...	Trend

SNP related genes (count: 2)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
GPR124	adhesion G protein-coupled receptor A2	8p11.22	Literature-origin; Mapped by Literature SNP
ADGRA2	adhesion G protein-coupled receptor A2	8p11.22	1(0/0/1)

SNPs in LD with rs113270504 (count: 0) View in gBrowse (chr8:37835186..37835186 )

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

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