Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1189348665
rs1189348665
F8
0.700 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002

dbSNP: rs1189348665
rs1189348665
F8
0.700 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002

dbSNP: rs1189348665
rs1189348665
F8
0.700 GeneticVariation UNIPROT Identification of seven novel mutations of F8C by DHPLC. 12203998

2002

dbSNP: rs1189348665
rs1189348665
F8
0.700 GeneticVariation UNIPROT Three novel point mutations causing haemophilia A. 12199686

2002

dbSNP: rs1208703993
rs1208703993
F8
0.700 GeneticVariation UNIPROT Three novel point mutations causing haemophilia A. 12199686

2002

dbSNP: rs1208703993
rs1208703993
F8
0.700 GeneticVariation UNIPROT Identification of seven novel mutations of F8C by DHPLC. 12203998

2002

dbSNP: rs1208703993
rs1208703993
F8
0.700 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002

dbSNP: rs1208703993
rs1208703993
F8
0.700 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002

dbSNP: rs1281943689
rs1281943689
F8
0.700 GeneticVariation UNIPROT Identification of seven novel mutations of F8C by DHPLC. 12203998

2002

dbSNP: rs1281943689
rs1281943689
F8
0.700 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002

dbSNP: rs1281943689
rs1281943689
F8
0.700 GeneticVariation UNIPROT Three novel point mutations causing haemophilia A. 12199686

2002

dbSNP: rs1281943689
rs1281943689
F8
0.700 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002

dbSNP: rs1290383918
rs1290383918
F8
0.700 GeneticVariation UNIPROT Identification of seven novel mutations of F8C by DHPLC. 12203998

2002

dbSNP: rs1290383918
rs1290383918
F8
0.700 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002

dbSNP: rs1290383918
rs1290383918
F8
0.700 GeneticVariation UNIPROT Three novel point mutations causing haemophilia A. 12199686

2002

dbSNP: rs1290383918
rs1290383918
F8
0.700 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002

dbSNP: rs1296842178
rs1296842178
F8
0.700 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002

dbSNP: rs1296842178
rs1296842178
F8
0.700 GeneticVariation UNIPROT Three novel point mutations causing haemophilia A. 12199686

2002

dbSNP: rs1296842178
rs1296842178
F8
0.700 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002

dbSNP: rs1296842178
rs1296842178
F8
0.700 GeneticVariation UNIPROT Identification of seven novel mutations of F8C by DHPLC. 12203998

2002

dbSNP: rs1312347909
rs1312347909
F8
0.700 GeneticVariation UNIPROT Identification of seven novel mutations of F8C by DHPLC. 12203998

2002

dbSNP: rs1312347909
rs1312347909
F8
0.700 GeneticVariation UNIPROT Three novel point mutations causing haemophilia A. 12199686

2002

dbSNP: rs1312347909
rs1312347909
F8
0.700 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002

dbSNP: rs1312347909
rs1312347909
F8
0.700 GeneticVariation UNIPROT Skewed X-chromosome inactivation in monochorionic diamniotic twin sisters results in severe and mild hemophilia A. 12351418

2002

dbSNP: rs1345538633
rs1345538633
F8
0.700 GeneticVariation UNIPROT 11 hemophilia A patients without mutations in the factor VIII encoding gene. 12195713

2002