Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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
Evidence status

HGVS name

10:g.111075832T>A

This variation has assays on 8 chips - click the plus to show

About this variant

This variant overlaps 1 transcript, has 2573 individual genotypes and is mentioned in 4 citations.

Variation displays