This variant has been flagged

  • None of the variant alleles match the reference allele (AT)
  • 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 (AT) at this location.
Location

Chromosome 19:10291947-10291948 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

Variant displays