Gene: WAS ×
Source: UNIPROT ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs132630272
rs132630272
WAS
0.700 GeneticVariation UNIPROT Absence of expression of the Wiskott-Aldrich syndrome protein in peripheral blood cells of Wiskott-Aldrich syndrome patients. 9683546

1998
dbSNP: rs132630273
rs132630273
WAS
0.700 GeneticVariation UNIPROT Absence of expression of the Wiskott-Aldrich syndrome protein in peripheral blood cells of Wiskott-Aldrich syndrome patients. 9683546

1998
dbSNP: rs139857045
rs139857045
WAS
0.700 GeneticVariation UNIPROT Absence of expression of the Wiskott-Aldrich syndrome protein in peripheral blood cells of Wiskott-Aldrich syndrome patients. 9683546

1998
dbSNP: rs146220228
rs146220228
WAS
0.700 GeneticVariation UNIPROT Absence of expression of the Wiskott-Aldrich syndrome protein in peripheral blood cells of Wiskott-Aldrich syndrome patients. 9683546

1998
dbSNP: rs132630272
rs132630272
WAS
0.700 GeneticVariation UNIPROT Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndrome. 9713366

1998
dbSNP: rs132630273
rs132630273
WAS
0.700 GeneticVariation UNIPROT Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndrome. 9713366

1998
dbSNP: rs139857045
rs139857045
WAS
0.700 GeneticVariation UNIPROT Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndrome. 9713366

1998
dbSNP: rs146220228
rs146220228
WAS
0.700 GeneticVariation UNIPROT Defective actin polymerization in EBV-transformed B-cell lines from patients with the Wiskott-Aldrich syndrome. 9713366

1998
dbSNP: rs132630272
rs132630272
WAS
0.700 GeneticVariation UNIPROT Identification of mutations in the Wiskott-Aldrich syndrome gene and characterization of a polymorphic dinucleotide repeat at DXS6940, adjacent to the disease gene. 7753869

1995
dbSNP: rs132630273
rs132630273
WAS
0.700 GeneticVariation UNIPROT Identification of mutations in the Wiskott-Aldrich syndrome gene and characterization of a polymorphic dinucleotide repeat at DXS6940, adjacent to the disease gene. 7753869

1995
dbSNP: rs139857045
rs139857045
WAS
0.700 GeneticVariation UNIPROT Identification of mutations in the Wiskott-Aldrich syndrome gene and characterization of a polymorphic dinucleotide repeat at DXS6940, adjacent to the disease gene. 7753869

1995
dbSNP: rs146220228
rs146220228
WAS
0.700 GeneticVariation UNIPROT Identification of mutations in the Wiskott-Aldrich syndrome gene and characterization of a polymorphic dinucleotide repeat at DXS6940, adjacent to the disease gene. 7753869

1995
dbSNP: rs132630272
rs132630272
WAS
0.700 GeneticVariation UNIPROT Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus. 8528198

1995
dbSNP: rs132630273
rs132630273
WAS
0.700 GeneticVariation UNIPROT Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus. 8528198

1995
dbSNP: rs139857045
rs139857045
WAS
0.700 GeneticVariation UNIPROT Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus. 8528198

1995
dbSNP: rs146220228
rs146220228
WAS
0.700 GeneticVariation UNIPROT Identification of WASP mutations in patients with Wiskott-Aldrich syndrome and isolated thrombocytopenia reveals allelic heterogeneity at the WAS locus. 8528198

1995
dbSNP: rs132630272
rs132630272
WAS
0.700 GeneticVariation UNIPROT Mutation analysis of five Japanese families with Wiskott-Aldrich syndrome and determination of the family members' carrier status using three different methods. 9098856

1997
dbSNP: rs132630273
rs132630273
WAS
0.700 GeneticVariation UNIPROT Mutation analysis of five Japanese families with Wiskott-Aldrich syndrome and determination of the family members' carrier status using three different methods. 9098856

1997
dbSNP: rs139857045
rs139857045
WAS
0.700 GeneticVariation UNIPROT Mutation analysis of five Japanese families with Wiskott-Aldrich syndrome and determination of the family members' carrier status using three different methods. 9098856

1997
dbSNP: rs146220228
rs146220228
WAS
0.700 GeneticVariation UNIPROT Mutation analysis of five Japanese families with Wiskott-Aldrich syndrome and determination of the family members' carrier status using three different methods. 9098856

1997
dbSNP: rs132630272
rs132630272
WAS
0.700 GeneticVariation UNIPROT Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes. 10447259

1999
dbSNP: rs132630273
rs132630273
WAS
0.700 GeneticVariation UNIPROT Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes. 10447259

1999
dbSNP: rs139857045
rs139857045
WAS
0.700 GeneticVariation UNIPROT Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes. 10447259

1999
dbSNP: rs146220228
rs146220228
WAS
0.700 GeneticVariation UNIPROT Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes. 10447259

1999
dbSNP: rs132630272
rs132630272
WAS
0.700 GeneticVariation UNIPROT Nuclear role of WASp in the pathogenesis of dysregulated TH1 immunity in human Wiskott-Aldrich syndrome. 20574068

2010