ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.55426G>C (p.Val18476Leu)

dbSNP: rs780649835
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
Eurofins Ntd Llc (ga) RCV000594127 SCV000705499 uncertain significance not provided 2017-01-23 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000594127 SCV001152870 uncertain significance not provided 2016-11-01 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000594127 SCV003819580 uncertain significance not provided 2019-10-21 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.