ClinVar Miner

Submissions for variant NM_001365951.3(KIF1B):c.5097-9C>T (rs376873833)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000860879 SCV001001053 benign Charcot-Marie-Tooth disease, type 2 2019-12-31 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173381 SCV001336469 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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