ClinVar Miner

Submissions for variant NM_015074.3(KIF1B):c.3285-15del (rs3215996)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000283128 SCV000346674 likely benign Neuroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Molecular Genetics Laboratory,London Health Sciences Centre RCV001173395 SCV001336483 benign Charcot-Marie-Tooth disease criteria provided, single submitter clinical testing
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV001286259 SCV001472798 benign none provided 2020-08-24 criteria provided, single submitter clinical testing

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