Original source

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

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

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

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

17:g.63475705C>A

About this variant

This variant overlaps 9 transcripts, 1 regulatory feature and has 2 sample genotypes.

Variant displays