ClinVar Miner

Submissions for variant NM_015074.3(KIF1B):c.*3911A>G (rs1138791)

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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 RCV000315156 SCV000346952 benign Charcot-Marie-Tooth disease, type 2 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000369878 SCV000346953 benign Neuroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000270484 SCV000346954 benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing

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