ClinVar Miner

Submissions for variant NM_001267550.2(TTN):c.12332C>G (p.Ala4111Gly) (rs140289517)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV000730353 SCV000526835 likely benign not provided 2021-06-24 criteria provided, single submitter clinical testing
Invitae RCV000528151 SCV000642657 uncertain significance Dilated cardiomyopathy 1G; Limb-girdle muscular dystrophy, type 2J 2017-06-27 criteria provided, single submitter clinical testing
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000730353 SCV000858082 uncertain significance not provided 2017-11-15 criteria provided, single submitter clinical testing

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