ClinVar Miner

List of variants reported as likely benign for Familial visceral amyloidosis, Ostertag type

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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_000239.3(LYZ):c.263C>A (p.Thr88Asn) rs1800973 0.04360
NM_021871.4(FGA):c.1542T>C (p.Pro514=) rs4766 0.00426
NM_000039.3(APOA1):c.284T>A (p.Phe95Tyr) rs138407155 0.00044
NM_021871.4(FGA):c.616C>G (p.Gln206Glu) rs560732073 0.00019
NM_000039.3(APOA1):c.*17C>T rs370532459 0.00014
NM_000039.3(APOA1):c.454G>A (p.Glu152Lys) rs574061789 0.00010
NM_021871.4(FGA):c.1444G>A (p.Val482Met) rs139146037 0.00006
NM_021871.4(FGA):c.1823G>C (p.Gly608Ala) rs370873387 0.00006
NM_000039.3(APOA1):c.-11G>A rs199729971 0.00005
NM_000039.3(APOA1):c.498C>A (p.Ser166Arg) rs757899657 0.00004
NM_000239.3(LYZ):c.156G>A (p.Trp52Ter) rs764263034 0.00004
NM_000239.3(LYZ):c.434G>A (p.Gly145Asp) rs762616173 0.00004
NM_000239.3(LYZ):c.272C>G (p.Ala91Gly) rs776898103 0.00003
NM_000039.3(APOA1):c.127G>C (p.Val43Leu) rs373545875
NM_000239.3(LYZ):c.*735del rs148802204

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