ClinVar Miner

List of variants in gene FGB reported as likely benign for coagulation protein disease

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
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HGVS dbSNP
NM_005141.4(FGB):c.*1369G>A rs2227426
NM_005141.4(FGB):c.*1517T>C rs2059502
NM_005141.4(FGB):c.*1617A>T rs2059503
NM_005141.4(FGB):c.*373G>A rs2227420
NM_005141.4(FGB):c.*443G>A rs2227422
NM_005141.4(FGB):c.*447T>C rs2227423
NM_005141.4(FGB):c.*918C>G rs2227424
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.1433G>A (p.Arg478Lys) rs4220
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.843G>T (p.Val281=) rs6058

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