ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.18303A>T (p.Val6101=)

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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 RCV002633299 SCV003516098 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-09-03 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003994508 SCV004813380 likely benign not specified 2024-02-11 criteria provided, single submitter clinical testing

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