ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.57345T>C (p.Tyr19115=)

dbSNP: rs879000172
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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 RCV001174747 SCV001338061 likely benign not specified 2020-01-11 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001450432 SCV001654039 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2022-09-14 criteria provided, single submitter clinical testing

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