ClinVar Miner

Submissions for variant NM_000313.4(PROS1):c.970T>C (p.Ser324Pro)

dbSNP: rs1576180280
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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 RCV000851920 SCV000900001 likely pathogenic Protein S deficiency disease 2019-02-01 criteria provided, single submitter research

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