ClinVar Miner

Submissions for variant NM_000488.4(SERPINC1):c.42-486_1154-846del

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Servicio de Hematología y Oncología médica, Universidad de Murcia RCV001779979 SCV002016217 pathogenic Hereditary antithrombin deficiency no assertion criteria provided research AntiFXa 52%; Ag 37%

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