ClinVar Miner

Submissions for variant NM_004006.2(DMD):c.3419A>G (p.His1140Arg) (rs201297190)

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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 RCV000723384 SCV000112479 uncertain significance not provided 2015-05-08 criteria provided, single submitter clinical testing
Invitae RCV001081258 SCV000560819 benign Duchenne muscular dystrophy 2019-12-31 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000723384 SCV000603376 benign not provided 2018-01-03 criteria provided, single submitter clinical testing

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