ClinVar Miner

Submissions for variant NM_015074.3(KIF1B):c.*3988G>A (rs571451087)

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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 RCV000337061 SCV000346964 likely benign Charcot-Marie-Tooth disease, type 2 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000400481 SCV000346965 likely benign Neuroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000292196 SCV000346966 likely benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing

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