ClinVar Miner

Submissions for variant NC_000001.11:g.173879820_173925989del

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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 RCV001779995 SCV002016233 pathogenic Hereditary antithrombin deficiency no assertion criteria provided research AntiFXa 44%; Ag 41%

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