ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.62547G>A (p.Thr20849=) (rs368969893)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Ambry Genetics RCV000247528 SCV000317974 likely benign Cardiovascular phenotype 2012-12-10 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000273812 SCV000339689 uncertain significance not provided 2016-03-03 criteria provided, single submitter clinical testing
Invitae RCV001086636 SCV000555581 likely benign Dilated cardiomyopathy 1G; Limb-girdle muscular dystrophy, type 2J 2019-12-31 criteria provided, single submitter clinical testing

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