ClinVar Miner

Submissions for variant NM_015074.3(KIF1B):c.168C>T (p.Tyr56=) (rs530566864)

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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 RCV000339224 SCV000346237 uncertain significance Neuroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000395463 SCV000346238 uncertain significance Charcot-Marie-Tooth disease, type 2 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000304740 SCV000346239 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing

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