ClinVar Miner

Submissions for variant NM_004006.2(DMD):c.6140A>G (p.Gln2047Arg) (rs773782786)

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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 RCV000328417 SCV000344714 benign not specified 2016-08-10 criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000328417 SCV000603372 benign not specified 2017-03-21 criteria provided, single submitter clinical testing
Invitae RCV000630585 SCV000751550 benign Duchenne muscular dystrophy 2019-12-31 criteria provided, single submitter clinical testing

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