ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.107377+13T>C

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003226877 SCV003923265 likely benign not specified 2024-12-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003779821 SCV004595522 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2023-06-05 criteria provided, single submitter clinical testing

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