ClinVar Miner

Submissions for variant NM_015074.3(KIF1B):c.720+17C>T (rs1339458)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000242299 SCV000312360 benign not specified criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173391 SCV001336479 benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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