This variation 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 (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
G/A | Ambiguity code: R | MAF: 0.03 (A)
Location

This variation maps to 3 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs115934919, rs3189761

HGVS name

None

Variation displays