ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.89187T>C (p.Ala29729=)

dbSNP: rs1401647603
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001669305 SCV001887131 likely benign not provided 2020-09-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073139 SCV002367626 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2023-07-25 criteria provided, single submitter clinical testing

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