ClinVar Miner

Submissions for variant NM_000132.4(F8):c.5883G>A (p.Trp1961Ter)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology RCV002281005 SCV002569315 pathogenic Hereditary factor VIII deficiency disease criteria provided, single submitter clinical testing

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