This variation has been flagged

  • None of the variant alleles match the reference allele (TT)
  • 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]

Note: The reference sequence for this variant (TTG) does not match the Ensembl reference sequence (TT) at this location.

Chromosome 6:32643422-32643423 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs9279937

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

About this variant

This variant overlaps 12 transcripts.

Variation displays