ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.5826A>C (p.Ala1942=)

dbSNP: rs1569558909
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000730009 SCV000857716 uncertain significance not provided 2017-10-27 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003512074 SCV004261339 likely benign Duchenne muscular dystrophy 2023-11-04 criteria provided, single submitter clinical testing

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