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 (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
C/G | Ambiguity code: S
Location

This variation maps to 2 genomic locations; None selected

HGVS name

None

Variation displays