ClinVar Miner

Submissions for variant NM_015074.3(KIF1B):c.184-6_184-5del (rs138324955)

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Total submissions: 6
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia RCV000254281 SCV000258078 benign not specified 2015-02-13 criteria provided, single submitter clinical testing
Invitae RCV000203918 SCV000261026 benign Charcot-Marie-Tooth disease, type 2 2017-07-31 criteria provided, single submitter clinical testing
PreventionGenetics,PreventionGenetics RCV000254281 SCV000312354 benign not specified criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000336206 SCV000346240 likely benign Pheochromocytoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000399328 SCV000346241 likely benign Neuroblastoma 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000203918 SCV000346242 likely benign Charcot-Marie-Tooth disease, type 2 2016-06-14 criteria provided, single submitter clinical testing

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