Gene: F9 ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1216516070
rs1216516070
F9
0.700 GeneticVariation UNIPROT Genetic determinants of immunogenicity to factor IX during the treatment of haemophilia B. 25470321

2015
dbSNP: rs1222227572
rs1222227572
F9
0.700 GeneticVariation UNIPROT Genetic determinants of immunogenicity to factor IX during the treatment of haemophilia B. 25470321

2015
dbSNP: rs1275708479
rs1275708479
F9
0.700 GeneticVariation UNIPROT Genetic determinants of immunogenicity to factor IX during the treatment of haemophilia B. 25470321

2015
dbSNP: rs143018900
rs143018900
F9
0.700 GeneticVariation UNIPROT Genetic determinants of immunogenicity to factor IX during the treatment of haemophilia B. 25470321

2015
dbSNP: rs1216516070
rs1216516070
F9
0.700 GeneticVariation UNIPROT Comprehensive analysis of phenotypes and genetics in 21 Chinese families with haemophilia B: characterization of five novel mutations. 25251685

2014
dbSNP: rs1222227572
rs1222227572
F9
0.700 GeneticVariation UNIPROT Comprehensive analysis of phenotypes and genetics in 21 Chinese families with haemophilia B: characterization of five novel mutations. 25251685

2014
dbSNP: rs1275708479
rs1275708479
F9
0.700 GeneticVariation UNIPROT Comprehensive analysis of phenotypes and genetics in 21 Chinese families with haemophilia B: characterization of five novel mutations. 25251685

2014
dbSNP: rs143018900
rs143018900
F9
0.700 GeneticVariation UNIPROT Comprehensive analysis of phenotypes and genetics in 21 Chinese families with haemophilia B: characterization of five novel mutations. 25251685

2014
dbSNP: rs1216516070
rs1216516070
F9
0.700 GeneticVariation UNIPROT Factor IX gene sequencing by a simple and sensitive 15-hour procedure for haemophilia B diagnosis: identification of two novel mutations. 11122099

2000
dbSNP: rs1222227572
rs1222227572
F9
0.700 GeneticVariation UNIPROT Factor IX gene sequencing by a simple and sensitive 15-hour procedure for haemophilia B diagnosis: identification of two novel mutations. 11122099

2000
dbSNP: rs1275708479
rs1275708479
F9
0.700 GeneticVariation UNIPROT Factor IX gene sequencing by a simple and sensitive 15-hour procedure for haemophilia B diagnosis: identification of two novel mutations. 11122099

2000
dbSNP: rs143018900
rs143018900
F9
0.700 GeneticVariation UNIPROT Factor IX gene sequencing by a simple and sensitive 15-hour procedure for haemophilia B diagnosis: identification of two novel mutations. 11122099

2000
dbSNP: rs1216516070
rs1216516070
F9
0.700 GeneticVariation UNIPROT Germline mutations in Peruvian patients with hemophilia B: pattern of mutation in AmerIndians is similar to the putative endogenous germline pattern. 9600455

1998
dbSNP: rs1216516070
rs1216516070
F9
0.700 GeneticVariation UNIPROT Five novel factor IX mutations in unrelated hemophilia B patients. 9452115

1998
dbSNP: rs1222227572
rs1222227572
F9
0.700 GeneticVariation UNIPROT Five novel factor IX mutations in unrelated hemophilia B patients. 9452115

1998
dbSNP: rs1222227572
rs1222227572
F9
0.700 GeneticVariation UNIPROT Germline mutations in Peruvian patients with hemophilia B: pattern of mutation in AmerIndians is similar to the putative endogenous germline pattern. 9600455

1998
dbSNP: rs1275708479
rs1275708479
F9
0.700 GeneticVariation UNIPROT Five novel factor IX mutations in unrelated hemophilia B patients. 9452115

1998
dbSNP: rs1275708479
rs1275708479
F9
0.700 GeneticVariation UNIPROT Germline mutations in Peruvian patients with hemophilia B: pattern of mutation in AmerIndians is similar to the putative endogenous germline pattern. 9600455

1998
dbSNP: rs143018900
rs143018900
F9
0.700 GeneticVariation UNIPROT Five novel factor IX mutations in unrelated hemophilia B patients. 9452115

1998
dbSNP: rs143018900
rs143018900
F9
0.700 GeneticVariation UNIPROT Germline mutations in Peruvian patients with hemophilia B: pattern of mutation in AmerIndians is similar to the putative endogenous germline pattern. 9600455

1998
dbSNP: rs1216516070
rs1216516070
F9
0.700 GeneticVariation UNIPROT Modification of the N-terminus of human factor IX by defective propeptide cleavage or acetylation results in a destabilized calcium-induced conformation: effects on phospholipid binding and activation by factor XIa. 9169594

1997
dbSNP: rs1222227572
rs1222227572
F9
0.700 GeneticVariation UNIPROT Modification of the N-terminus of human factor IX by defective propeptide cleavage or acetylation results in a destabilized calcium-induced conformation: effects on phospholipid binding and activation by factor XIa. 9169594

1997
dbSNP: rs1275708479
rs1275708479
F9
0.700 GeneticVariation UNIPROT Modification of the N-terminus of human factor IX by defective propeptide cleavage or acetylation results in a destabilized calcium-induced conformation: effects on phospholipid binding and activation by factor XIa. 9169594

1997
dbSNP: rs143018900
rs143018900
F9
0.700 GeneticVariation UNIPROT Modification of the N-terminus of human factor IX by defective propeptide cleavage or acetylation results in a destabilized calcium-induced conformation: effects on phospholipid binding and activation by factor XIa. 9169594

1997
dbSNP: rs1216516070
rs1216516070
F9
0.700 GeneticVariation UNIPROT Twenty-five novel mutations of the factor IX gene in haemophilia B. 8680410

1995