ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.6858-15dup

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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 RCV003830482 SCV004632134 benign Charcot-Marie-Tooth disease axonal type 2O 2023-12-12 criteria provided, single submitter clinical testing

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