This variation has been flagged

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

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


Chromosome 11:17352480-17352483 (forward strand) | View in location tab

Most severe consequence

Archive dbSNP rs72560114

This variation has 25 HGVS names - click the plus to show

Variation displays