ClinVar Miner

Submissions for variant NM_007078.3(LDB3):c.1305T>C (p.Pro435=)

dbSNP: rs1009984915
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
CHEO Genetics Diagnostic Laboratory, Children's Hospital of Eastern Ontario RCV001799332 SCV002043370 benign Cardiomyopathy 2019-08-14 criteria provided, single submitter clinical testing
Institute of Human Genetics, University of Wuerzburg RCV004596486 SCV005088683 not provided Hypertrophic cardiomyopathy 2 no assertion 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.