ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.15975G>T (p.Leu5325=)

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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 RCV002584074 SCV002940500 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-10-21 criteria provided, single submitter clinical testing
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV004587362 SCV005076739 likely benign not specified 2024-04-10 criteria provided, single submitter clinical testing

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