ClinVar Miner

Submissions for variant NM_000091.5(COL4A3):c.260C>T (p.Thr87Met)

gnomAD frequency: 0.00009  dbSNP: rs377136253
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001904832 SCV002120076 likely benign not provided 2024-08-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV005005314 SCV002791529 uncertain significance Autosomal dominant Alport syndrome; Hematuria, benign familial, 2; Alport syndrome 3b, autosomal recessive 2024-03-27 criteria provided, single submitter 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.