ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.74608G>C (p.Ala24870Pro)

dbSNP: rs768892376
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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 RCV000471212 SCV000542882 uncertain significance Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2016-10-15 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003139635 SCV003821129 uncertain significance not provided 2019-07-01 criteria provided, single submitter clinical testing

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