This variation has been flagged

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

A/G | Ambiguity code: R
Note: The reference sequence for this variant (A) does not match the Ensembl reference sequence (GG) at this location.

Chromosome 18:23698008-23698009 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs79702875

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

About this variant

This variant overlaps 6 transcripts and has 4 individual genotypes.

Variation displays