SNP Report

Basic Info
Name rs150738695 dbSNP Ensembl
Location chr4:271758 - 271758(1)
Variant Alleles A/G
Ancestral Allele A
Minor Allele G
Minor Allele Frequence 0.00958466
Functional Annotation missense_variant; upstream_gene_variant.
Polyphen Annotation: probably damaging(ENST00000419098, ENST00000619749)
SIFT Annotation: deleterious(ENST00000419098, ENST00000619749)
Consequence to Transcript missense_variant(ENST00000419098, ENST00000619749); upstream_gene_variant(ENST00000507882, ENST00000511111)
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 A/G GERP=0.977 GERP=0.977 Putative damaging exonic variants found in the five linkage ...... Putative damaging exonic variants found in the five linkage regions. More... Trend

SNP related genes (count: 1)
Approved Symbol Approved Name Location No. of Studies (Positive/Negative/Trend)
ZNF732 zinc finger protein 732 4p16.3 1(0/0/1)

SNPs in LD with rs150738695 (count: 0) View in gBrowse (chr4:271758..271758 )

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

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