Gene: F9 ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852241
rs137852241
F9
0.800 GeneticVariation UNIPROT

dbSNP: rs137852247
rs137852247
F9
0.800 GeneticVariation UNIPROT

dbSNP: rs137852254
rs137852254
F9
0.800 GeneticVariation UNIPROT

dbSNP: rs137852257
rs137852257
F9
0.800 GeneticVariation UNIPROT

dbSNP: rs1170838100
rs1170838100
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs1175050951
rs1175050951
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs1182648920
rs1182648920
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs1233706534
rs1233706534
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs1243180674
rs1243180674
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs1303221289
rs1303221289
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs1306658513
rs1306658513
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs1330705989
rs1330705989
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs137852225
rs137852225
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs137852242
rs137852242
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs1385141619
rs1385141619
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs1410080079
rs1410080079
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs757996262
rs757996262
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs767828752
rs767828752
F9
0.700 GeneticVariation UNIPROT

dbSNP: rs387906481
rs387906481
F9
0.800 GeneticVariation UNIPROT Identification of the molecular defect in factor IX Chapel Hill: substitution of histidine for arginine at position 145. 6603618

1983
dbSNP: rs1216516070
rs1216516070
F9
0.700 GeneticVariation UNIPROT Identification of the molecular defect in factor IX Chapel Hill: substitution of histidine for arginine at position 145. 6603618

1983
dbSNP: rs1222227572
rs1222227572
F9
0.700 GeneticVariation UNIPROT Identification of the molecular defect in factor IX Chapel Hill: substitution of histidine for arginine at position 145. 6603618

1983
dbSNP: rs1275708479
rs1275708479
F9
0.700 GeneticVariation UNIPROT Identification of the molecular defect in factor IX Chapel Hill: substitution of histidine for arginine at position 145. 6603618

1983
dbSNP: rs143018900
rs143018900
F9
0.700 GeneticVariation UNIPROT Identification of the molecular defect in factor IX Chapel Hill: substitution of histidine for arginine at position 145. 6603618

1983
dbSNP: rs387906481
rs387906481
F9
0.800 GeneticVariation UNIPROT Genetic defect responsible for the dysfunctional protein: factor IXLong Beach. 3401602

1988
dbSNP: rs1216516070
rs1216516070
F9
0.700 GeneticVariation UNIPROT Genetic defect responsible for the dysfunctional protein: factor IXLong Beach. 3401602

1988