ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.76788G>T (p.Val25596=)

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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 RCV003795410 SCV004578739 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2023-06-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711968 SCV005259428 likely benign not provided criteria provided, single submitter not provided

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