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|Ambiguity code: R|MAF: 0.47 (A)
Location

This variant maps to 3 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs62079737

HGVS name

None

About this variant

This variant has 2507 sample genotypes.

Variant displays