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]

C/T | Ambiguity code: Y

This variation maps to 6 genomic locations; None selected

Evidence status

HGVS name


About this variant

This variant has 24 individual genotypes.

Variation displays