ClinVar Miner

List of variants reported as likely pathogenic for Familial visceral amyloidosis, Ostertag type; Congenital afibrinogenemia; Familial dysfibrinogenemia by Fulgent Genetics, Fulgent Genetics

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_021871.4(FGA):c.364+1G>A	rs778779380	0.00001
NM_000508.3(FGA):c.1717C>T (p.Arg573Cys)	rs121909613
NM_021871.4(FGA):c.922C>T (p.Arg308Ter)	rs776817952

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