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]

-/AA | Ancestral: A

Chromosome 7:103865133 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs67238793, rs67238792

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

About this variant

This variant overlaps 6 transcripts and has 2 individual genotypes.

Variation displays