ClinVar Miner

Submissions for variant NM_004006.2(DMD):c.2645G>A (p.Gly882Asp) (rs228406)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Athena Diagnostics Inc RCV000576731 SCV000677274 benign Becker muscular dystrophy; Duchenne muscular dystrophy 2017-04-28 criteria provided, single submitter clinical testing
GeneDx RCV000124736 SCV000168173 benign not specified 2013-11-14 criteria provided, single submitter clinical testing This variant is considered likely benign or benign based on one or more of the following criteria: it is a conservative change, it occurs at a poorly conserved position in the protein, it is predicted to be benign by multiple in silico algorithms, and/or has population frequency not consistent with disease.
Integrated Genetics/Laboratory Corporation of America RCV000124736 SCV000919268 benign not specified 2018-07-19 criteria provided, single submitter clinical testing
Invitae RCV000206108 SCV000262123 benign Duchenne muscular dystrophy 2018-01-05 criteria provided, single submitter clinical testing

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