Gene: WAS ×
Source: CURATED ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs132630268
rs132630268
WAS
T 0.710 CausalMutation CLINVAR

dbSNP: rs1057517845
rs1057517845
WAS
A 0.700 CausalMutation CLINVAR

dbSNP: rs1057520700
rs1057520700
WAS
C 0.700 CausalMutation CLINVAR

dbSNP: rs132630271
rs132630271
WAS
T 0.700 CausalMutation CLINVAR

dbSNP: rs1557006354
rs1557006354
WAS
T 0.700 CausalMutation CLINVAR

dbSNP: rs1557006672
rs1557006672
WAS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs1557007035
rs1557007035
WAS
G 0.700 GeneticVariation CLINVAR

dbSNP: rs193922414
rs193922414
WAS
T 0.700 GeneticVariation CLINVAR

dbSNP: rs193922415
rs193922415
WAS
T 0.700 CausalMutation CLINVAR

dbSNP: rs193922416
rs193922416
WAS
AC 0.700 GeneticVariation CLINVAR

dbSNP: rs587776742
rs587776742
WAS
T 0.700 CausalMutation CLINVAR

dbSNP: rs587776743
rs587776743
WAS
AGACGAG 0.700 CausalMutation CLINVAR

dbSNP: rs587776744
rs587776744
WAS
A 0.700 CausalMutation CLINVAR

dbSNP: rs587776745
rs587776745
WAS
T 0.700 CausalMutation CLINVAR

dbSNP: rs1557007123
rs1557007123
WAS
T 0.700 CausalMutation CLINVAR The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene. 7579347

1995
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: rs132630268
rs132630268
WAS
A 0.710 CausalMutation CLINVAR Isolation of a novel gene mutated in Wiskott-Aldrich syndrome. 8069912

1994
dbSNP: rs132630268
rs132630268
WAS
A 0.710 CausalMutation CLINVAR 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 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