Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 17:63475705 (forward strand) | View in location tab

Most severe consequence
HGVS name

17:g.63475705C>A

About this variant

This variant overlaps 10 transcripts and has 2 individual genotypes.

Variation displays