ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.69716-9C>T

dbSNP: rs776930347
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001403253 SCV001605118 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-08-04 criteria provided, single submitter clinical testing
GeneDx RCV001547995 SCV001767835 likely benign not provided 2020-01-07 criteria provided, single submitter clinical testing

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