Original source

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

T/A | Ancestral: A | Ambiguity code: W | MAF: 0.35 (T)

Chromosome 17:63476833 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS name


About this variant

This variant overlaps 9 transcripts, 1 regulatory feature, has 2504 sample genotypes and is mentioned in 35 citations.

Variant displays