ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.103207C>T (p.Leu34403=) (rs773892755)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000243672 SCV000315637 likely benign not specified criteria provided, single submitter clinical testing
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000725875 SCV000340179 uncertain significance not provided 2016-03-30 criteria provided, single submitter clinical testing
GeneDx RCV000725875 SCV000519024 likely benign not provided 2020-01-15 criteria provided, single submitter clinical testing
Invitae RCV000559465 SCV000642531 likely benign Dilated cardiomyopathy 1G; Limb-girdle muscular dystrophy, type 2J 2020-04-23 criteria provided, single submitter clinical testing

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