Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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 rs386541188, rs58713577

HGVS name

8:g.116618444A>C

This variant has assays on 13 chips - click the plus to show

About this variant

This variant has 2512 sample genotypes, is associated with 2 phenotypes and is mentioned in 64 citations.

Variant displays