ClinVar Miner

Submissions for variant NM_000504.4(F10):c.535C>T (p.Arg179Cys)

gnomAD frequency: 0.00001  dbSNP: rs1277295882
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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 RCV000852155 SCV000899795 uncertain significance Hereditary factor X deficiency disease 2019-02-01 criteria provided, single submitter research

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