Original source

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

Alleles
G/C/T|Ancestral: G|Ambiguity code: B|MAF: 0.05 (T)
Location

Chromosome 20:58651037 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

Variant displays