ClinVar Miner

Submissions for variant NM_001365951.3(KIF1B):c.*249CA[13]

dbSNP: rs111663673
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000326562 SCV000346769 uncertain significance Charcot-Marie-Tooth disease type 2 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000381078 SCV000346770 uncertain significance Neuroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000267787 SCV000346771 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing

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