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
A/C | Ancestral: A | Ambiguity code: M
Location

This variation maps to 3 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs36217412

HGVS name

None

Variation displays