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]

AAAG/- | Ancestral: A
Note: The reference base for this variant (AAAG) does not match the Ensembl reference base (A) at this location.

Chromosome 5:96775265 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs34915580

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

About this variant

This variant overlaps 48 transcripts and has 1 individual genotype.

Variation displays