ClinVar Miner

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

Included ClinVar conditions (43):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_005141.4(FGB):c.*1550C>T rs1044291
NM_005141.4(FGB):c.*422A>C rs2227421
NM_005141.4(FGB):c.*619T>C rs2227439
NM_005141.4(FGB):c.*834del rs57313183
NM_005141.4(FGB):c.567C>T (p.Ser189=) rs6056
NM_005141.4(FGB):c.959-13_959-10del rs140114081

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