WAS, WASP actin nucleation promoting factor, 7454

N. diseases: 204; N. variants: 37
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs132630273
rs132630273
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C1839163
Disease:
THROMBOCYTOPENIA 1 (disorder) 		T 0.810 CausalMutation CLINVAR
dbSNP: rs132630274
rs132630274
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C1845987
Disease:
Neutropenia, Severe Congenital, X-Linked 		C 0.810 CausalMutation CLINVAR
dbSNP: rs132630268
rs132630268
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C0043194
Disease:
Wiskott-Aldrich Syndrome 		T 0.710 CausalMutation CLINVAR
dbSNP: rs1057517845
rs1057517845
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C1845987
Disease:
Neutropenia, Severe Congenital, X-Linked 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1057517845
rs1057517845
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C1839163
Disease:
THROMBOCYTOPENIA 1 (disorder) 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1057517845
rs1057517845
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C0043194
Disease:
Wiskott-Aldrich Syndrome 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1057520700
rs1057520700
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C0043194
Disease:
Wiskott-Aldrich Syndrome 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1057520700
rs1057520700
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C0000731
Disease:
Abdomen distended 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1057520700
rs1057520700
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C0025222
Disease:
Melena 		C 0.700 CausalMutation CLINVAR
dbSNP: rs132630269
rs132630269
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C1839163
Disease:
THROMBOCYTOPENIA 1 (disorder) 		T 0.700 CausalMutation CLINVAR
dbSNP: rs132630270
rs132630270
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C1839163
Disease:
THROMBOCYTOPENIA 1 (disorder) 		G 0.700 CausalMutation CLINVAR
dbSNP: rs132630271
rs132630271
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C0043194
Disease:
Wiskott-Aldrich Syndrome 		T 0.700 CausalMutation CLINVAR
dbSNP: rs132630272
rs132630272
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C4016481
Disease:
WISKOTT-ALDRICH SYNDROME, ATTENUATED 		C 0.700 CausalMutation CLINVAR
dbSNP: rs132630275
rs132630275
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C1839164
Disease:
Thrombocytopenia, X-Linked, Intermittent 		G 0.700 CausalMutation CLINVAR
dbSNP: rs132630276
rs132630276
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C1839164
Disease:
Thrombocytopenia, X-Linked, Intermittent 		A 0.700 CausalMutation CLINVAR
dbSNP: rs1557006354
rs1557006354
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C1845987
Disease:
Neutropenia, Severe Congenital, X-Linked 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1557006354
rs1557006354
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C1839163
Disease:
THROMBOCYTOPENIA 1 (disorder) 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1557006354
rs1557006354
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C0043194
Disease:
Wiskott-Aldrich Syndrome 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1557006672
rs1557006672
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C0043194
Disease:
Wiskott-Aldrich Syndrome 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1557007035
rs1557007035
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C0043194
Disease:
Wiskott-Aldrich Syndrome 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1557007165
rs1557007165
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C1845987
Disease:
Neutropenia, Severe Congenital, X-Linked 		A 0.700 CausalMutation CLINVAR
dbSNP: rs193922414
rs193922414
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C0043194
Disease:
Wiskott-Aldrich Syndrome 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs193922415
rs193922415
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C0043194
Disease:
Wiskott-Aldrich Syndrome 		T 0.700 CausalMutation CLINVAR
dbSNP: rs193922416
rs193922416
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C0043194
Disease:
Wiskott-Aldrich Syndrome 		AC 0.700 GeneticVariation CLINVAR
dbSNP: rs387906716
rs387906716
Entrez Id: 7454
Gene Symbol: WAS
WAS
CUI: C1845987
Disease:
Neutropenia, Severe Congenital, X-Linked 		C 0.700 CausalMutation CLINVAR