ClinVar Miner

Submissions for variant NM_001365951.3(KIF1B):c.*4664_*4665insG

dbSNP: rs571589510
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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 RCV000262609 SCV000346994 uncertain significance Charcot-Marie-Tooth disease type 2 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000301314 SCV000346995 uncertain significance Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000367666 SCV000346996 uncertain significance Neuroblastoma 2016-06-14 criteria provided, single submitter clinical testing

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