This variant maps to 2 locations

Select a location:
Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.44 (A)
Location

This variant maps to 2 genomic locations; None selected

Evidence status

Clinical significance

HGVS name

None

This variant has assays on 9 chips - click the plus to show

About this variant

This variant overlaps 1 regulatory feature, has 2512 sample genotypes, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays