Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.39 (G)
Location

Chromosome 10:23191389 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58290468

HGVS name

10:g.23191389G>A

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 1 transcript and has 3690 sample genotypes.

Variant displays