ClinVar Miner

List of variants studied for Familial dysfibrinogenemia by Institute of Human Genetics, University Hospital Muenster

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Total variants: 3
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HGVS dbSNP gnomAD frequency
NM_005141.5(FGB):c.749A>G (p.Glu250Gly) rs759800033 0.00003
NM_005141.5(FGB):c.811G>T (p.Asp271Tyr) rs913936601
NM_021871.4(FGA):c.117del (p.Val40fs) rs762964798

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