ClinVar Miner

Submissions for variant NM_005141.5(FGB):c.284G>A (p.Cys95Tyr)

dbSNP: rs2110761933
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genetics and Molecular Pathology, SA Pathology RCV002272673 SCV002556656 uncertain significance Familial dysfibrinogenemia 2019-12-13 criteria provided, single submitter clinical testing

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