ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.75099C>T (p.Asp25033=) (rs370272814)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000591231 SCV000706746 uncertain significance not provided 2017-03-05 criteria provided, single submitter clinical testing
Invitae RCV000591231 SCV000765446 likely benign not provided 2018-11-26 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000591231 SCV001248649 uncertain significance not provided 2020-01-01 criteria provided, single submitter clinical testing
Invitae RCV001394349 SCV001596032 likely benign Dilated cardiomyopathy 1G; Limb-girdle muscular dystrophy, type 2J 2020-09-04 criteria provided, single submitter clinical testing

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