ClinVar Miner

Submissions for variant NM_015074.3(KIF1B):c.1905-10_1905-9del (rs58344165)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics, Eurofins Clinical Diagnostics RCV000176097 SCV000227695 uncertain significance not provided 2015-02-27 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173382 SCV001336470 likely benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing

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