ClinVar Miner

Submissions for variant NM_030777.4(SLC2A10):c.918C>T (p.Leu306=)

dbSNP: rs1979909437
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Women's Health and Genetics/Laboratory Corporation of America, LabCorp RCV001192795 SCV001361147 likely benign not specified 2019-10-21 criteria provided, single submitter clinical testing
Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+ RCV001724265 SCV001955630 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001724265 SCV001964573 likely benign not provided no assertion criteria provided clinical testing

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