ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.26201-20C>A

gnomAD frequency: 0.00001  dbSNP: rs761178461
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001670843 SCV001883916 benign not provided 2015-12-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073124 SCV002367540 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-01-19 criteria provided, single submitter clinical testing

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