ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.36405G>A (p.Val12135=) (rs373815877)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001257059 SCV000555473 likely benign Dilated cardiomyopathy 1G; Limb-girdle muscular dystrophy, type 2J 2019-12-31 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000469135 SCV001152952 uncertain significance not provided 2016-12-01 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001287351 SCV001474026 likely benign none provided 2020-03-06 criteria provided, single submitter clinical testing

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