Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has assays on 10 chips - click the plus to show

About this variant

This variant has 3967 sample genotypes.

Variant displays