ClinVar Miner

Submissions for variant NM_176787.5(PIGN):c.1251+11C>T

gnomAD frequency: 0.00571  dbSNP: rs141918272
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 RCV001518564 SCV001727284 benign Multiple congenital anomalies-hypotonia-seizures syndrome 1 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001549738 SCV001769947 likely benign not provided 2018-07-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001549738 SCV005210788 likely 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.