ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.67637-4A>G (rs376053678)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000723876 SCV000203697 uncertain significance not provided 2017-06-16 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000245132 SCV000315537 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV001087495 SCV001007161 likely benign Dilated cardiomyopathy 1G; Limb-girdle muscular dystrophy, type 2J 2020-11-17 criteria provided, single submitter clinical testing

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