Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909607
rs121909607
FGA
T 0.700 CausalMutation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs143648758
rs143648758
F11
A 0.700 CausalMutation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs148685782
rs148685782
FGG
C 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs201007090
rs201007090
F11 ; F11-AS1
A 0.700 CausalMutation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs36209567
rs36209567
F7
T 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs6054
rs6054
FGB
T 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs61748477
rs61748477
VWF
A 0.700 GeneticVariation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs62643632
rs62643632
VWF
C 0.700 CausalMutation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs756908183
rs756908183
F11
T 0.700 CausalMutation CLINVAR Diagnostic high-throughput sequencing of 2396 patients with bleeding, thrombotic, and platelet disorders. 31064749

2019
dbSNP: rs1057518837
rs1057518837
ITGB3
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1057518838
rs1057518838
ITGB3
G 0.700 GeneticVariation CLINVAR

dbSNP: rs61750072
rs61750072
VWF
T 0.700 CausalMutation CLINVAR

dbSNP: rs869320714
rs869320714
SLFN14
T 0.700 GeneticVariation CLINVAR

dbSNP: rs869320715
rs869320715
SLFN14
A 0.700 GeneticVariation CLINVAR