Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W|MAF: 0.43 (A)
Location

Chromosome 10:111075832 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

10:g.111075832T>A

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 1 transcript, has 2900 sample genotypes and is mentioned in 5 citations.

Variant displays