ClinVar Miner

Submissions for variant NM_001005361.3(DNM2):c.235+13G>A

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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 RCV002636758 SCV003507012 likely benign Charcot-Marie-Tooth disease dominant intermediate B 2025-01-21 criteria provided, single submitter clinical testing

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