ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.104943A>G (p.Glu34981=) (rs372312805)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000246183 SCV000315646 likely benign not specified criteria provided, single submitter clinical testing
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000725662 SCV000338464 uncertain significance not provided 2018-09-12 criteria provided, single submitter clinical testing
Invitae RCV001087016 SCV000765304 likely benign Dilated cardiomyopathy 1G; Limb-girdle muscular dystrophy, type 2J 2020-10-05 criteria provided, single submitter clinical testing

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