ClinVar Miner

List of variants in gene FGA studied for abdominal and pelvic region disorder

Included ClinVar conditions (891):
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Gene type:
ClinVar version:
Total variants: 25
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HGVS dbSNP
NM_000508.4(FGA):c.1622del (p.Val541Alafs) rs587777761
NM_000508.4(FGA):c.1629del (p.Thr544Leufs) rs587777762
NM_000508.4(FGA):c.1634A>T (p.Glu545Val) rs121909612
NM_000508.4(FGA):c.1718G>T (p.Arg573Leu) rs78506343
NM_000508.4(FGA):c.2089G>A (p.Gly697Ser) rs771023837
NM_000508.4(FGA):c.991A>G (p.Thr331Ala) rs6050
NM_021871.3(FGA):c.*50T>G rs369606098
NM_021871.3(FGA):c.-58A>G rs2070011
NM_021871.3(FGA):c.1199C>T (p.Ser400Phe) rs184635235
NM_021871.3(FGA):c.1417G>A (p.Asp473Asn) rs200378626
NM_021871.3(FGA):c.1444G>A (p.Val482Met) rs139146037
NM_021871.3(FGA):c.1542T>C (p.Pro514=) rs4766
NM_021871.3(FGA):c.16A>G (p.Ile6Val) rs2070025
NM_021871.3(FGA):c.1823G>C (p.Gly608Ala) rs370873387
NM_021871.3(FGA):c.1838A>G (p.His613Arg) rs201686865
NM_021871.3(FGA):c.244A>C (p.Thr82Pro) rs199554805
NM_021871.3(FGA):c.346G>A (p.Asp116Asn) rs886059153
NM_021871.3(FGA):c.450G>A (p.Gln150=) rs368446857
NM_021871.3(FGA):c.614A>G (p.Glu205Gly) rs886059152
NM_021871.3(FGA):c.616C>G (p.Gln206Glu) rs560732073
NM_021871.3(FGA):c.666A>T (p.Pro222=) rs886059151
NM_021871.3(FGA):c.765G>A (p.Pro255=) rs779582722
NM_021871.3(FGA):c.822C>T (p.Ser274=) rs886059150
NM_021871.3(FGA):c.904C>G (p.Pro302Ala) rs200203992
NM_021871.3(FGA):c.919A>G (p.Asn307Asp) rs750564329

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