ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.94431G>A (p.Leu31477=)

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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 RCV003331657 SCV004038647 likely benign not specified 2023-08-19 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003777387 SCV004592644 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2023-03-26 criteria provided, single submitter clinical testing

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