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: C | Ambiguity code: M
Location

This variation maps to 8 genomic locations; None selected

Evidence status

Synonyms
HGVS name

None

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays