ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.9636C>G (p.Val3212=) (rs2295445)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000866610 SCV001007732 benign not provided 2018-10-23 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173863 SCV001336979 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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