Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.41 (A)
Location

Chromosome 1:2961801 (forward strand)|View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

Synonyms

Archive dbSNP rs61128345

HGVS name

1:g.2961801G>A

Genotyping chips

This variant has assays on 10 chips - Show

About this variant

This variant has 3967 sample genotypes.

Variant displays