ClinVar Miner

Submissions for variant NM_000488.4(SERPINC1):c.790G>C (p.Glu264Gln)

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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 RCV003313853 SCV004013036 uncertain significance Hereditary antithrombin deficiency criteria provided, single submitter clinical testing

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