Original source

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

Alleles
C/A/G|Ancestral: G|Ambiguity code: V|MAF: 0.18 (A)
Location

Chromosome 17:63919146 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

About this variant

Variant displays