Original source

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

Alleles
A/G|Ancestral: G|Ambiguity code: R|MAF: 0.17 (G)
Location

Chromosome 12:48765827 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

12:g.48765827A>G

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

Variant displays