Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W
Location

Chromosome 17:7281339 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

17:g.7281339A>T

About this variant

Variant displays