ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.66464-15A>G

gnomAD frequency: 0.00002  dbSNP: rs769254613
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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 RCV002075484 SCV002374904 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-01-17 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004711780 SCV005259450 likely benign not provided criteria provided, single submitter not provided

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