This variant 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 (release 144)|View in dbSNP

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs79702875

HGVS names

This variant has 7 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and has 4 sample genotypes.

Variant displays