Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121965064
rs121965064
F11
C 0.810 CausalMutation CLINVAR Factor XI deficiency in Ashkenazi Jews in Israel. 2052060

1991

dbSNP: rs121965064
rs121965064
F11
0.810 GeneticVariation UNIPROT Factor XI (plasma thromboplastin antecedent) deficiency in Ashkenazi Jews is a bleeding disorder that can result from three types of point mutations. 2813350

1989

dbSNP: rs121965064
rs121965064
F11
C 0.810 CausalMutation CLINVAR Factor XI (plasma thromboplastin antecedent) deficiency in Ashkenazi Jews is a bleeding disorder that can result from three types of point mutations. 2813350

1989

dbSNP: rs121965064
rs121965064
F11
C 0.810 GeneticVariation CLINVAR

dbSNP: rs139695003
rs139695003
T 0.800 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019

dbSNP: rs281875245
rs281875245
F11
T 0.800 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019

dbSNP: rs281875257
rs281875257
F11
A 0.800 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019

dbSNP: rs281875272
rs281875272
F11
G 0.800 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019

dbSNP: rs281875275
rs281875275
A 0.800 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019

dbSNP: rs28934608
rs28934608
F11
T 0.800 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019

dbSNP: rs28934609
rs28934609
A 0.800 CausalMutation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019

dbSNP: rs121965065
rs121965065
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs121965067
rs121965067
F11
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs121965068
rs121965068
F11
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs121965069
rs121965069
F11
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs121965070
rs121965070
F11
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs121965071
rs121965071
F11
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs121965072
rs121965072
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs139695003
rs139695003
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs1554083754
rs1554083754
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs281875245
rs281875245
F11
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs281875250
rs281875250
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs281875251
rs281875251
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs281875257
rs281875257
F11
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015

dbSNP: rs281875272
rs281875272
F11
0.800 GeneticVariation UNIPROT Molecular basis and bleeding manifestations of factor XI deficiency in 11 Turkish families. 25158988

2015