ClinVar Miner

Submissions for variant NM_006267.5(RANBP2):c.2351G>A (p.Arg784Lys) (rs2912838)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Pediatric Genomic Medicine,Children's Mercy Hospital and Clinics RCV000514780 SCV000610610 likely benign not provided 2017-08-31 criteria provided, single submitter clinical testing
Invitae RCV001085448 SCV000646783 benign Encephalopathy, acute, infection-induced, 3, suceptibility to 2020-12-02 criteria provided, single submitter clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV000514780 SCV001797818 likely benign not provided no assertion criteria provided clinical testing

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