ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.65142C>G (p.Val21714=)

dbSNP: rs1575973571
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute RCV000845345 SCV000987393 likely benign not provided criteria provided, single submitter clinical testing
Invitae RCV001484326 SCV001688743 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2019-12-27 criteria provided, single submitter clinical testing

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