ClinVar Miner

Submissions for variant NM_000504.4(F10):c.1325G>A (p.Gly442Asp)

dbSNP: rs1233330150
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV001420418 SCV001622550 uncertain significance Factor X deficiency 2021-04-28 criteria provided, single submitter research
Birmingham Platelet Group; University of Birmingham RCV001270526 SCV001450825 likely pathogenic Abnormal bleeding; Thrombocytopenia 2020-05-01 no assertion criteria provided research

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