ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.1537-20dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003802648 SCV004591676 benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2022-11-17 criteria provided, single submitter clinical testing

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