SNP Report

Basic Info

Name	rs7386782 dbSNP Ensembl
Location	chr8:132041062 - 132041062(1)
Variant Alleles	T/C
Ancestral Allele	C
Minor Allele	T
Minor Allele Frequence	0.26238
Functional Annotation	missense_variant. Polyphen Annotation: benign(ENST00000254627, ENST00000262283) SIFT Annotation: tolerated(ENST00000254627, ENST00000262283)
Consequence to Transcript	missense_variant(ENST00000254627, ENST00000262283)
No. of Studies	0 (Positive: 0; Negative: 0; Trend: 0)
Source	LD-proxy

SNP related studies (count: 0)

SNP related genes (count: 1)

Approved Symbol	Approved Name	Location	No. of Studies (Positive/Negative/Trend)
OC90	otoconin 90	8q24.22	1(0/1/0)

SNPs in LD with rs7386782 (count: 0) View in gBrowse (chr8:132041062..132041062 )

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

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