This variation has been flagged

  • None of the variant alleles match the reference allele (AT)
  • Mapped position is not compatible with reported alleles
Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/G | Ambiguity code: R
Note: The reference sequence for this variant (A) does not match the Ensembl reference sequence (AT) at this location.
Location

Chromosome 19:10291947-10291948 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 5 HGVS names - click the plus to show

Variation displays