This variation has been flagged

  • Variation has more than 3 different alleles
  • Flagged as suspect by dbSNP
Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

G/A/C/T | Ancestral: G | Ambiguity code: N | MAF: < 0.01 (A)

Chromosome 19:5831970 (forward strand) | View in location tab

Most severe consequence
Evidence status


This variation has 18 HGVS names - click the plus to show

Variation displays