ClinVar Miner

Submissions for variant NM_001365951.3(KIF1B):c.*4279dup

dbSNP: rs531640427
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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 RCV000360547 SCV000346976 likely benign Neuroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000261208 SCV000346977 likely benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000316247 SCV000346978 likely benign Charcot-Marie-Tooth disease type 2 2016-06-14 criteria provided, single submitter clinical testing

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