ClinVar Miner

Submissions for variant NM_001042492.2(NF1):c.[6708delT;6710C>G]

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital RCV001002748 SCV001146936 pathogenic Neurofibromatosis, type 1 2020-01-23 criteria provided, single submitter clinical testing

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