ClinVar Miner

List of variants reported as uncertain significance for Familial dysfibrinogenemia by Institute of Human Genetics, University Hospital Muenster

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Total variants: 2

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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

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