ClinVar Miner

Submissions for variant NC_000001.11:g.173908412_173919816dup

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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 RCV001822079 SCV002064259 pathogenic Hereditary antithrombin deficiency no assertion criteria provided research AntiFXa 61%; Ag 46%

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