This variation has been flagged

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

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

Alleles
-/AAAC | Ancestral: A
Location

Chromosome 7:100776575 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs112428808

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

Variation displays