Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
Evidence status

HGVS name

17:g.63476833T>A

About this variant

This variant overlaps 10 transcripts, has 2504 individual genotypes and is mentioned in 35 citations.

Variation displays