Original source

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

Alleles
C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.26 (C)
Location

Chromosome 17:63476980 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.63476980C>T

About this variant

This variant overlaps 10 transcripts, has 2506 individual genotypes and is mentioned in 1 citation.

Variation displays