ClinVar Miner

Submissions for variant NM_000313.4(PROS1):c.1568T>C (p.Met523Thr)

dbSNP: rs1483547708
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ISTH-SSC Genomics in Thrombosis and Hemostasis, KU Leuven, Center for Molecular and Vascular Biology RCV002245348 SCV002515539 uncertain significance Protein S deficiency disease no assertion criteria provided clinical testing

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