ClinVar Miner

List of variants in gene FGB reported as uncertain significance for coagulation protein disease

Included ClinVar conditions (69):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 64
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HGVS dbSNP gnomAD frequency
NM_005141.5(FGB):c.794C>T (p.Pro265Leu) rs6054 0.00275
NM_005141.5(FGB):c.*846T>G rs541828079 0.00166
NM_005141.5(FGB):c.*233G>T rs539731011 0.00154
NM_005141.5(FGB):c.298C>T (p.Pro100Ser) rs2227434 0.00134
NM_005141.5(FGB):c.115-12C>T rs187641148 0.00058
NM_005141.5(FGB):c.*450T>A rs183181144 0.00053
NM_005141.5(FGB):c.1244+7G>A rs142937995 0.00038
NM_005141.5(FGB):c.*624C>T rs754198978 0.00034
NM_005141.5(FGB):c.*1671C>T rs765773409 0.00032
NM_005141.5(FGB):c.*1771C>T rs776780011 0.00026
NM_005141.5(FGB):c.*592G>A rs376470048 0.00019
NM_005141.5(FGB):c.*1687A>G rs992721102 0.00014
NM_005141.5(FGB):c.*1738G>A rs760784701 0.00014
NM_005141.5(FGB):c.*363A>G rs545671394 0.00013
NM_005141.5(FGB):c.*1105A>G rs542187592 0.00012
NM_005141.5(FGB):c.200G>C (p.Ser67Thr) rs371842822 0.00011
NM_005141.5(FGB):c.*1372T>A rs371670019 0.00009
NM_005141.5(FGB):c.*1444C>A rs886059145 0.00006
NM_005141.5(FGB):c.*304G>A rs901759260 0.00005
NM_005141.5(FGB):c.752C>T (p.Thr251Ile) rs776988939 0.00004
NM_005141.5(FGB):c.*1542T>C rs886059146 0.00003
NM_005141.5(FGB):c.*15A>G rs375561591 0.00003
NM_005141.5(FGB):c.*1867T>C rs886059148 0.00003
NM_005141.5(FGB):c.*303C>T rs886059142 0.00003
NM_005141.5(FGB):c.4A>G (p.Lys2Glu) rs6053 0.00003
NM_005141.5(FGB):c.749A>G (p.Glu250Gly) rs759800033 0.00003
NM_005141.5(FGB):c.*464C>T rs940820346 0.00002
NM_005141.5(FGB):c.*526C>T rs933339992 0.00002
NM_005141.5(FGB):c.251A>C (p.Lys84Thr) rs886059141 0.00002
NM_005141.5(FGB):c.*1019G>T rs1478189415 0.00001
NM_005141.5(FGB):c.*1892G>A rs765456260 0.00001
NM_005141.5(FGB):c.*36A>G rs758231685 0.00001
NM_005141.5(FGB):c.*427G>A rs1196345013 0.00001
NM_005141.5(FGB):c.-6_-5del rs757727864 0.00001
NM_005141.5(FGB):c.103G>A (p.Asp35Asn) rs747783086 0.00001
NM_005141.5(FGB):c.332A>G (p.Gln111Arg) rs758080375 0.00001
NM_005141.5(FGB):c.564T>C (p.Asn188=) rs759250713 0.00001
NM_005141.5(FGB):c.656A>G (p.Gln219Arg) rs778766319 0.00001
NM_005141.5(FGB):c.659T>C (p.Met220Thr) rs1363577874 0.00001
NM_005141.5(FGB):c.762G>A (p.Met254Ile) rs201536638 0.00001
NM_005141.5(FGB):c.80T>C (p.Leu27Pro) rs1442627097 0.00001
NM_005141.5(FGB):c.*1204T>C rs1447745807
NM_005141.5(FGB):c.*1252A>C rs1730444171
NM_005141.5(FGB):c.*1409C>A rs886059144
NM_005141.5(FGB):c.*1544T>C rs886059147
NM_005141.5(FGB):c.*1639T>C rs1026178982
NM_005141.5(FGB):c.*1998A>G rs886059149
NM_005141.5(FGB):c.*277A>G rs1466304617
NM_005141.5(FGB):c.*361A>T rs886059143
NM_005141.5(FGB):c.*496G>A rs557290052
NM_005141.5(FGB):c.*801A>G rs1578787077
NM_005141.5(FGB):c.*835del rs768727295
NM_005141.5(FGB):c.114+11del rs779228767
NM_005141.5(FGB):c.1292G>T (p.Gly431Val) rs779328318
NM_005141.5(FGB):c.1330G>A (p.Gly444Ser)
NM_005141.5(FGB):c.169C>T (p.Pro57Ser) rs971404907
NM_005141.5(FGB):c.210C>T (p.Gly70=) rs933834957
NM_005141.5(FGB):c.254T>C (p.Val85Ala) rs775809959
NM_005141.5(FGB):c.284G>A (p.Cys95Tyr) rs2110761933
NM_005141.5(FGB):c.419C>A (p.Thr140Asn)
NM_005141.5(FGB):c.506T>A (p.Val169Asp) rs2110768107
NM_005141.5(FGB):c.691T>C (p.Cys231Arg) rs1730226269
NM_005141.5(FGB):c.811G>T (p.Asp271Tyr) rs913936601
NM_005141.5(FGB):c.946T>C (p.Cys316Arg)

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