Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

Alleles
A/C|Ancestral: A|Ambiguity code: M|MAF: 0.08 (C)
Location

Chromosome 8:116618444 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs58713577, rs386541188

HGVS name

8:g.116618444A>C

Genotyping chips

This variant has assays on 13 chips - Show

About this variant

This variant has 4180 sample genotypes, is associated with 2 phenotypes and is mentioned in 69 citations.

Variant displays