Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.02 (A)
Location

Chromosome 17:7281077 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

17:g.7281077C>A

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

Variant displays