ClinVar Miner

Submissions for variant NM_000488.4(SERPINC1):c.409-12del

dbSNP: rs201656611
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Total submissions: 2
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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 RCV002222133 SCV002499589 uncertain significance Hereditary antithrombin deficiency criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002222133 SCV004450971 benign Hereditary antithrombin deficiency 2023-12-28 criteria provided, single submitter clinical testing

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