ClinVar Miner

List of variants reported as uncertain significance for hematologic disorder by Knight Diagnostic Laboratories, Oregon Health and Sciences University

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 4
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001994.3(F13B):c.1163A>T (p.Glu388Val) rs5991 0.00175
NM_152564.5(VPS13B):c.983A>G (p.His328Arg) rs181625846 0.00053
NM_000312.4(PROC):c.580C>T (p.Arg194Cys) rs371071104 0.00004
NM_001018115.3(FANCD2):c.3962G>C (p.Arg1321Pro) rs147205530

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.