ClinVar Miner

List of variants in gene FGA reported as benign for Familial visceral amyloidosis, Ostertag type

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Total variants: 19
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HGVS dbSNP gnomAD frequency
NM_021871.3(FGA):c.-58A>G rs2070011 0.65406
NM_021871.4(FGA):c.991A>G (p.Thr331Ala) rs6050 0.29256
NM_021871.4(FGA):c.1366A>G (p.Thr456Ala) rs2070031 0.00262
NM_021871.4(FGA):c.16A>G (p.Ile6Val) rs2070025 0.00250
NM_021871.4(FGA):c.181-14C>T rs190703077 0.00240
NM_021871.4(FGA):c.300G>A (p.Lys100=) rs112877216 0.00240
NM_021871.4(FGA):c.1417G>A (p.Asp473Asn) rs200378626 0.00048
NM_021871.4(FGA):c.1199C>T (p.Ser400Phe) rs184635235 0.00031
NM_021871.4(FGA):c.244A>C (p.Thr82Pro) rs199554805 0.00031
NM_021871.4(FGA):c.*50T>G rs369606098 0.00010
NM_021871.4(FGA):c.1072G>A (p.Gly358Arg) rs201105899 0.00007
NM_021871.4(FGA):c.1838A>G (p.His613Arg) rs201686865 0.00004
NM_021871.4(FGA):c.1718G>A (p.Arg573His) rs78506343 0.00003
NM_021871.4(FGA):c.1918C>G (p.Pro640Ala) rs199571440 0.00002
NM_021871.4(FGA):c.450G>A (p.Gln150=) rs368446857 0.00002
NM_021871.4(FGA):c.904C>G (p.Pro302Ala) rs200203992 0.00002
NM_021871.4(FGA):c.1912G>A (p.Gly638Arg) rs771429165 0.00001
NM_000508.5(FGA):c.2587del (p.Leu863_Val864insTer) rs773678959
NM_021871.4(FGA):c.*133G>A rs182736373

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