ClinVar Miner

Submissions for variant NM_021871.4(FGA):c.364+5G>A

dbSNP: rs891744509
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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 RCV002222136 SCV002499607 uncertain significance Congenital afibrinogenemia criteria provided, single submitter clinical testing

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