ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.10626+7A>G (rs1427174553)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000871892 SCV001013620 likely benign not provided 2018-08-20 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173870 SCV001336986 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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