ClinVar Miner

Submissions for variant NM_001379286.1(ZNF423):c.1869G>A (p.Pro623=)

gnomAD frequency: 0.02845  dbSNP: rs16947741
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000246032 SCV000312332 benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000529787 SCV000652406 benign Nephronophthisis 14 2024-01-31 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV000529787 SCV002514224 benign Nephronophthisis 14 2021-12-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004714594 SCV005289755 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.