Original source

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

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

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

Most severe consequence
 
Regulatory region variant
Evidence status

Synonyms

Archive dbSNP rs56552070, rs58359063

HGVS name

10:g.100101678G>A

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 5 citations.

Variant displays