Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.10 (A)
Location

Chromosome 17:58167894 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

17:g.58167894G>A

About this variant

This variant overlaps 1 transcript and has 2505 sample genotypes.

Variant displays