Original source

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

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

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

Most severe consequence
Upstream gene variant
Evidence status

HGVS name


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