ClinVar Miner

List of variants reported as uncertain significance for hematologic disorder by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000975.5(RPL11):c.508-9_508-5del
NM_001258392.3(CLPB):c.979G>T (p.Val327Leu)

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.