ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.86822-8T>G

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 7
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Baylor Genetics RCV003147843 SCV003834908 uncertain significance Hypertrophic cardiomyopathy 9 2021-01-15 criteria provided, single submitter clinical testing
Baylor Genetics RCV003147845 SCV003835194 uncertain significance Tibial muscular dystrophy 2021-01-15 criteria provided, single submitter clinical testing
Baylor Genetics RCV003147848 SCV003835269 uncertain significance Early-onset myopathy with fatal cardiomyopathy 2021-03-05 criteria provided, single submitter clinical testing
Baylor Genetics RCV003147847 SCV003835301 uncertain significance Myopathy, myofibrillar, 9, with early respiratory failure 2021-01-15 criteria provided, single submitter clinical testing
Baylor Genetics RCV003147844 SCV003835404 uncertain significance Dilated cardiomyopathy 1G 2021-01-15 criteria provided, single submitter clinical testing
Baylor Genetics RCV003147846 SCV003836163 uncertain significance Autosomal recessive limb-girdle muscular dystrophy type 2J 2021-01-15 criteria provided, single submitter clinical testing
Invitae RCV003778885 SCV004576201 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2023-07-17 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.