ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.79281C>T (p.Asp26427=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV003312506 SCV004011256 likely benign not provided 2023-04-01 criteria provided, single submitter clinical testing TTN: BP4, BP7
Labcorp Genetics (formerly Invitae), Labcorp RCV005227983 SCV005867012 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2024-03-13 criteria provided, single submitter clinical testing

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