ClinVar Miner

Submissions for variant NM_020884.7(MYH7B):c.4415G>A (p.Arg1472Gln)

gnomAD frequency: 0.00001  dbSNP: rs1417887060
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Division of Cardiology, Departments of Internal Medicine and Genetic Diagnosis Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology RCV000991031 SCV000930671 likely pathogenic Hypertrophic cardiomyopathy 1 2019-06-20 no assertion criteria provided case-control

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.