ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.1959T>C (p.Asn653=)

gnomAD frequency: 0.00001  dbSNP: rs770238198
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001733386 SCV001983570 likely benign not specified 2021-09-26 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002073982 SCV002480891 likely benign Duchenne muscular dystrophy 2024-07-11 criteria provided, single submitter clinical testing

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