ClinVar Miner

Submissions for variant NM_001927.4(DES):c.640-10C>T

gnomAD frequency: 0.00001  dbSNP: rs750812904
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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 RCV001485824 SCV001690272 likely benign Desmin-related myofibrillar myopathy 2022-03-18 criteria provided, single submitter clinical testing

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