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

Alleles
-/AA | Ancestral: A
Location

Chromosome 7:103647547 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs72594234, rs80137106

This variation has 7 HGVS names - click the plus to show

Variation displays