ClinVar Miner

List of variants in gene FGB studied for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
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HGVS dbSNP
NM_005141.4(FGB):c.*1369G>A rs2227426
NM_005141.4(FGB):c.*1372T>A rs371670019
NM_005141.4(FGB):c.*1409C>A rs886059144
NM_005141.4(FGB):c.*1444C>A rs886059145
NM_005141.4(FGB):c.*1517T>C rs2059502
NM_005141.4(FGB):c.*1542T>C rs886059146
NM_005141.4(FGB):c.*1544T>C rs886059147
NM_005141.4(FGB):c.*1550C>T rs1044291
NM_005141.4(FGB):c.*15A>G rs375561591
NM_005141.4(FGB):c.*1617A>T rs2059503
NM_005141.4(FGB):c.*1671C>T rs765773409
NM_005141.4(FGB):c.*1738G>A rs760784701
NM_005141.4(FGB):c.*1771C>T rs776780011
NM_005141.4(FGB):c.*1867T>C rs886059148
NM_005141.4(FGB):c.*1998A>G rs886059149
NM_005141.4(FGB):c.*303C>T rs886059142
NM_005141.4(FGB):c.*361A>T rs886059143
NM_005141.4(FGB):c.*36A>G rs758231685
NM_005141.4(FGB):c.*373G>A rs2227420
NM_005141.4(FGB):c.*422A>C rs2227421
NM_005141.4(FGB):c.*443G>A rs2227422
NM_005141.4(FGB):c.*447T>C rs2227423
NM_005141.4(FGB):c.*496G>A rs557290052
NM_005141.4(FGB):c.*592G>A rs376470048
NM_005141.4(FGB):c.*619T>C rs2227439
NM_005141.4(FGB):c.*624C>T rs754198978
NM_005141.4(FGB):c.*834del rs57313183
NM_005141.4(FGB):c.*835del rs768727295
NM_005141.4(FGB):c.*918C>G rs2227424
NM_005141.4(FGB):c.-6_-5del rs757727864
NM_005141.4(FGB):c.1113A>G (p.Ser371=) rs6057
NM_005141.4(FGB):c.1125C>T (p.Tyr375=) rs4681
NM_005141.4(FGB):c.114+11del rs779228767
NM_005141.4(FGB):c.1148T>G (p.Leu383Arg) rs121909621
NM_005141.4(FGB):c.1244+1G>T rs606231224
NM_005141.4(FGB):c.1244+7G>A rs142937995
NM_005141.4(FGB):c.1289G>A (p.Gly430Asp) rs121909622
NM_005141.4(FGB):c.139C>T (p.Arg47Ter) rs121909625
NM_005141.4(FGB):c.1433G>A (p.Arg478Lys) rs4220
NM_005141.4(FGB):c.200G>C (p.Ser67Thr) rs371842822
NM_005141.4(FGB):c.251A>C (p.Lys84Thr) rs886059141
NM_005141.4(FGB):c.291C>T (p.His97=) rs6060
NM_005141.4(FGB):c.318T>C (p.Cys106=) rs6055
NM_005141.4(FGB):c.332A>G (p.Gln111Arg) rs758080375
NM_005141.4(FGB):c.4A>G (p.Lys2Glu) rs6053
NM_005141.4(FGB):c.564T>C (p.Asn188=) rs759250713
NM_005141.4(FGB):c.567C>T (p.Ser189=) rs6056
NM_005141.4(FGB):c.605T>A (p.Leu202Gln) rs121909624
NM_005141.4(FGB):c.794C>T (p.Pro265Leu) rs6054
NM_005141.4(FGB):c.843G>T (p.Val281=) rs6058
NM_005141.4(FGB):c.958+13C>T rs606231223
NM_005141.4(FGB):c.959-13_959-10del rs140114081

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