ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.2508T>C (p.Tyr836=)

dbSNP: rs886044674
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000381239 SCV000345880 uncertain significance not provided 2016-09-14 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000536795 SCV000625873 likely benign Duchenne muscular dystrophy 2024-10-22 criteria provided, single submitter clinical testing
Natera, Inc. RCV001833417 SCV002089719 likely benign Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency 2018-06-13 no assertion criteria provided clinical testing

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