ClinVar Miner

Submissions for variant NM_018668.4(VPS33B):c.240-13_240-12del (rs111274092)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics,PreventionGenetics RCV000245562 SCV000313254 benign not specified 2016-02-09 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000405825 SCV000394461 likely benign Arthrogryposis with renal dysfunction and cholestasis syndrome 2016-06-14 criteria provided, single submitter clinical testing
Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen RCV000245562 SCV001740543 benign not specified no assertion criteria provided clinical testing

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