This variation has been flagged

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

C/G | Ambiguity code: S
Note: The reference sequence for this variant (C) does not match the Ensembl reference sequence (GC) at this location.

Chromosome 1:153259680-153259681 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs762577

HGVS name


About this variant

This variant overlaps 2 transcripts and has 154 individual genotypes.

Variation displays