ClinVar Miner

Submissions for variant NM_144696.6(AXDND1):c.3032-3597T>C (rs2274622)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000354410 SCV000351491 likely benign Steroid-resistant nephrotic syndrome 2016-06-14 criteria provided, single submitter clinical testing
Human Genetics Disease in Children – Taif University,Taif University RCV000210053 SCV000265976 benign Nephrotic syndrome, idiopathic, steroid-resistant 2016-01-01 no assertion criteria provided clinical testing

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.