Gene: VWF ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs41276738
rs41276738
VWF
0.810 GeneticVariation UNIPROT

dbSNP: rs61749370
rs61749370
VWF
0.800 GeneticVariation UNIPROT C1272F: a novel type 2A von Willebrand's disease mutation in A1 domain; its clinical significance. 21592258

2012
dbSNP: rs61749384
rs61749384
VWF
0.800 GeneticVariation UNIPROT C1272F: a novel type 2A von Willebrand's disease mutation in A1 domain; its clinical significance. 21592258

2012
dbSNP: rs61749397
rs61749397
VWF
0.800 GeneticVariation UNIPROT C1272F: a novel type 2A von Willebrand's disease mutation in A1 domain; its clinical significance. 21592258

2012
dbSNP: rs61750072
rs61750072
VWF
0.800 GeneticVariation UNIPROT C1272F: a novel type 2A von Willebrand's disease mutation in A1 domain; its clinical significance. 21592258

2012
dbSNP: rs61749370
rs61749370
VWF
0.800 GeneticVariation UNIPROT Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease. 8622978

1996
dbSNP: rs61749384
rs61749384
VWF
0.800 GeneticVariation UNIPROT Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease. 8622978

1996
dbSNP: rs61749397
rs61749397
VWF
0.800 GeneticVariation UNIPROT Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease. 8622978

1996
dbSNP: rs61750072
rs61750072
VWF
0.800 GeneticVariation UNIPROT Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand disease. 8622978

1996
dbSNP: rs61749370
rs61749370
VWF
0.800 GeneticVariation UNIPROT Effects of different amino-acid substitutions in the leucine 694-proline 708 segment of recombinant von Willebrand factor. 8547152

1995
dbSNP: rs61749370
rs61749370
VWF
0.800 GeneticVariation UNIPROT Identification of two mutations (Arg611Cys and Arg611His) in the A1 loop of von Willebrand factor (vWF) responsible for type 2 von Willebrand disease with decreased platelet-dependent function of vWF. 7620154

1995
dbSNP: rs61749370
rs61749370
VWF
0.800 GeneticVariation UNIPROT Identification of a candidate missense mutation in a family with von Willebrand disease type IIC. 7789955

1995
dbSNP: rs61749384
rs61749384
VWF
0.800 GeneticVariation UNIPROT Identification of a candidate missense mutation in a family with von Willebrand disease type IIC. 7789955

1995
dbSNP: rs61749384
rs61749384
VWF
0.800 GeneticVariation UNIPROT Effects of different amino-acid substitutions in the leucine 694-proline 708 segment of recombinant von Willebrand factor. 8547152

1995
dbSNP: rs61749384
rs61749384
VWF
0.800 GeneticVariation UNIPROT Identification of two mutations (Arg611Cys and Arg611His) in the A1 loop of von Willebrand factor (vWF) responsible for type 2 von Willebrand disease with decreased platelet-dependent function of vWF. 7620154

1995
dbSNP: rs61749397
rs61749397
VWF
0.800 GeneticVariation UNIPROT Effects of different amino-acid substitutions in the leucine 694-proline 708 segment of recombinant von Willebrand factor. 8547152

1995
dbSNP: rs61749397
rs61749397
VWF
0.800 GeneticVariation UNIPROT Identification of two mutations (Arg611Cys and Arg611His) in the A1 loop of von Willebrand factor (vWF) responsible for type 2 von Willebrand disease with decreased platelet-dependent function of vWF. 7620154

1995
dbSNP: rs61749397
rs61749397
VWF
0.800 GeneticVariation UNIPROT Identification of a candidate missense mutation in a family with von Willebrand disease type IIC. 7789955

1995
dbSNP: rs61750072
rs61750072
VWF
0.800 GeneticVariation UNIPROT Identification of a candidate missense mutation in a family with von Willebrand disease type IIC. 7789955

1995
dbSNP: rs61750072
rs61750072
VWF
0.800 GeneticVariation UNIPROT Effects of different amino-acid substitutions in the leucine 694-proline 708 segment of recombinant von Willebrand factor. 8547152

1995
dbSNP: rs61750072
rs61750072
VWF
0.800 GeneticVariation UNIPROT Identification of two mutations (Arg611Cys and Arg611His) in the A1 loop of von Willebrand factor (vWF) responsible for type 2 von Willebrand disease with decreased platelet-dependent function of vWF. 7620154

1995
dbSNP: rs61749370
rs61749370
VWF
0.800 GeneticVariation UNIPROT Investigation of type IIC von Willebrand disease. 8011991

1994
dbSNP: rs61749370
rs61749370
VWF
0.800 GeneticVariation UNIPROT Leu 697-->Val mutation in mature von Willebrand factor is responsible for type IIB von Willebrand disease. 8123843

1994
dbSNP: rs61749384
rs61749384
VWF
0.800 GeneticVariation UNIPROT Investigation of type IIC von Willebrand disease. 8011991

1994
dbSNP: rs61749384
rs61749384
VWF
0.800 GeneticVariation UNIPROT Leu 697-->Val mutation in mature von Willebrand factor is responsible for type IIB von Willebrand disease. 8123843

1994