ClinVar Miner

Submissions for variant NM_001365951.3(KIF1B):c.78C>T (p.Cys26=) (rs772548887)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000863209 SCV001003829 likely benign Charcot-Marie-Tooth disease, type 2 2019-12-31 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001172596 SCV001335659 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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