Original source

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

Alleles
C/A/T|Ancestral: C|Ambiguity code: H|MAF: 0.01 (T)
Location

Chromosome 19:48394029 (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