ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.74871G>A (p.Lys24957=)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV003236310 SCV003934092 likely benign not specified 2023-05-15 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003779857 SCV004608359 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2023-10-23 criteria provided, single submitter clinical testing

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