ClinVar Miner

Submissions for variant NC_000001.11:g.173914640_173922032del

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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 RCV001779976 SCV002016214 pathogenic Hereditary antithrombin deficiency no assertion criteria provided research AntiFXa 53%; Ag 46%

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