Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.21 (A)

Chromosome 10:100101678 (forward strand) | View in location tab

Most severe consequence
Regulatory region variant
Evidence status


Archive dbSNP rs56552070, rs58359063

HGVS name


Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant overlaps 2 regulatory features, has 3613 sample genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variant displays