This variation has been flagged

  • None of the variant alleles match the reference allele (G)
  • 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
-/CCCGGGTGAGGGCGGG | Ancestral: G
Location

Chromosome 22:23262729 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs60132635, rs3833377

This variation has 9 HGVS names - click the plus to show

Variation displays