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

This variation maps to 8 genomic locations; None selected

Evidence status

HGVS name

None

This variation has assays on 12 chips - click the plus to show

Variation displays