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


Chromosome 11:17330933-17330936 (forward strand) | View in location tab

Most severe consequence

Archive dbSNP rs72560114

This variation has 29 HGVS names - click the plus to show

About this variant

This variant overlaps 18 transcripts.

Variation displays