ClinVar Miner

Submissions for variant NM_000504.4(F10):c.837C>A (p.Tyr279Ter)

dbSNP: rs1250509122
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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 RCV002245496 SCV002515800 pathogenic Hereditary factor X deficiency disease no assertion criteria provided research

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