This variant has been flagged

None of the variant alleles match the reference allele

Select a location:
Original source

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

Alleles
G/A|Ancestral: G|Ambiguity code: R|MAF: 0.43 (A)
Location

This variant maps to 6 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

Genotyping chips

This variant has assays on 11 chips - Show

About this variant

This variant overlaps 2 regulatory features, has 3698 sample genotypes and is mentioned in 9 citations.

Variant displays