ClinVar Miner

Submissions for variant NM_005141.5(FGB):c.811G>T (p.Asp271Tyr)

dbSNP: rs913936601
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, University Hospital Muenster RCV002210933 SCV002496145 uncertain significance Familial dysfibrinogenemia 2022-01-20 criteria provided, single submitter clinical testing ACMG categories: PM2,PP3

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