ClinVar Miner

Submissions for variant NM_000130.5(F5):c.986G>A (p.Cys329Tyr)

dbSNP: rs574459300
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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 RCV002245398 SCV002515631 uncertain significance Factor V deficiency no assertion criteria provided research

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