ClinVar Miner

Submissions for variant NM_000504.4(F10):c.1210T>C (p.Cys404Arg)

dbSNP: rs1595099645
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
NIHR Bioresource Rare Diseases, University of Cambridge RCV000851584 SCV000899300 likely pathogenic Hereditary factor X deficiency disease 2019-02-01 criteria provided, single submitter research

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