Original source

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

T/A | Ancestral: A | Ambiguity code: W | MAF: 0.19 (T)

Chromosome 6:31617223 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 8 transcripts, 1 regulatory feature, has 3985 sample genotypes, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays