ClinVar Miner

Submissions for variant NM_014625.4(NPHS2):c.873+10C>T

gnomAD frequency: 0.00019  dbSNP: rs536934083
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 RCV000928082 SCV001073685 benign not provided 2024-03-04 criteria provided, single submitter clinical testing
Natera, Inc. RCV001276835 SCV001463418 uncertain significance Steroid-resistant nephrotic syndrome 2020-04-24 no assertion criteria provided clinical testing
PreventionGenetics, part of Exact Sciences RCV003960467 SCV004775659 likely benign NPHS2-related disorder 2020-03-17 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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.