ClinVar Miner

List of variants studied for Fine-Lubinsky syndrome

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 3
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001128225.3(SLC39A13):c.682G>C (p.Asp228His) rs781198913
NM_001395413.1(POR):c.1484G>C (p.Arg495Pro) rs782104882
NM_005336.6(HDLBP):c.1731+1G>A rs2533259787

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.