This variation has been flagged

  • None of the variant alleles match the reference allele
  • Mapped position is not compatible with reported alleles
Select a location:
Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
A/C | Ambiguity code: M
Location

This variation maps to 7 genomic locations; None selected

Evidence status

Synonyms

Archive dbSNP rs112222934

HGVS name

None

Variation displays