ClinVar Miner

Submissions for variant NM_001927.4(DES):c.210G>A (p.Arg70=)

dbSNP: rs761255472
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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 RCV001490896 SCV001695470 likely benign Desmin-related myofibrillar myopathy 2022-03-08 criteria provided, single submitter clinical testing

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