ClinVar Miner

Submissions for variant NM_000312.4(PROC):c.532G>C (p.Ala178Pro)

dbSNP: rs1254257945
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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 RCV000852153 SCV000899793 likely pathogenic Reduced protein C activity 2019-02-01 criteria provided, single submitter research

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