This variation has been flagged

  • None of the variant alleles match the reference allele (TT)
  • 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/T | Ambiguity code: W
Note: The reference sequence for this variant (A) does not match the Ensembl reference sequence (TT) at this location.
Location

Chromosome 5:68254847-68254848 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1643921

This variation has 9 HGVS names - click the plus to show

Variation displays