ClinVar Miner

Submissions for variant NC_000001.11:g.173905922_173905923ins[NC_000006.11:56893618_56896059]

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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 RCV001779993 SCV002016231 pathogenic Hereditary antithrombin deficiency no assertion criteria provided research AntiFXa 56%; Ag 61%

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