This variation has been flagged

  • None of the variant alleles match the reference allele (C)
  • 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
-/TC/TCTT/TCTTTCTTTCTTTCTT | Ancestral: C
Location

Chromosome 2:112838770 (forward strand) | View in location tab

Co-located

with dbSNP rs5021469 (C/T)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs66954505, rs66954506

This variation has 3 HGVS names - click the plus to show

Variation displays