ClinVar Miner

Submissions for variant NM_004006.2(DMD):c.1687C>T (p.Arg563Cys) (rs145739725)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000362270 SCV000343976 uncertain significance not provided 2016-07-29 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000766091 SCV000897566 uncertain significance Becker muscular dystrophy; Duchenne muscular dystrophy; Dilated cardiomyopathy 3B 2018-10-31 criteria provided, single submitter clinical testing
Invitae RCV000362270 SCV001004898 likely benign not provided 2019-02-25 criteria provided, single submitter clinical testing

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