ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.75642C>T (p.Ile25214=)

dbSNP: rs1559390679
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000734666 SCV000862823 uncertain significance not provided 2018-08-13 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002536526 SCV003485494 likely benign Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J 2023-06-30 criteria provided, single submitter clinical testing

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