ClinVar Miner

Submissions for variant NM_015352.2(POFUT1):c.964C>T (p.Leu322Phe)

gnomAD frequency: 0.04125  dbSNP: rs17268666
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000557054 SCV000654188 benign Dowling-Degos disease 2 2024-01-22 criteria provided, single submitter clinical testing
GeneDx RCV001672855 SCV001884193 benign not provided 2019-07-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001672855 SCV005315043 benign not provided criteria provided, single submitter not provided

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.