ClinVar Miner

Submissions for variant NM_004006.3(DMD):c.10761G>A (p.Glu3587=)

dbSNP: rs2147933829
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002127166 SCV002404915 likely benign Duchenne muscular dystrophy 2021-04-24 criteria provided, single submitter clinical testing

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