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
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.40 (G)
Location

This variant maps to 10 genomic locations; None selected

Evidence status

HGVS name

None

About this variant

This variant has 2508 sample genotypes.

Variant displays