WAS, WASP actin nucleation promoting factor, 7454

N. diseases: 204; N. variants: 37
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs387906717
rs387906717 		0.827 0.120 X 48688403 missense variant T/C snv
CUI: C0023530
Disease: Leukopenia
Leukopenia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs387906717
rs387906717 		0.827 0.120 X 48688403 missense variant T/C snv
CUI: C3463824
Disease: MYELODYSPLASTIC SYNDROME
MYELODYSPLASTIC SYNDROME 		Hemic and Lymphatic Diseases 0.010 1.000 1 2010 2010
dbSNP: rs387906717
rs387906717 		0.827 0.120 X 48688403 missense variant T/C snv
CUI: C0027947
Disease: Neutropenia
Neutropenia 		Hemic and Lymphatic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs387906717
rs387906717 		0.827 0.120 X 48688403 missense variant T/C snv
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases 0.010 1.000 1 2009 2009
dbSNP: rs387906717
rs387906717 		0.827 0.120 X 48688403 missense variant T/C snv
CUI: C0026985
Disease: Myelodysplasia
Myelodysplasia 		0.010 1.000 1 2010 2010
dbSNP: rs387906717
rs387906717 		0.827 0.120 X 48688403 missense variant T/C snv
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
Neutropenia, Severe Congenital, X-Linked 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 0
dbSNP: rs132630268
rs132630268 		0.882 0.120 X 48684407 missense variant G/A;C;T snv
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases 0.710 1.000 19 1994 2013
dbSNP: rs782290433
rs782290433 		0.882 0.120 X 48684373 missense variant G/A snv 5.5E-06
CUI: C1839163
Disease: THROMBOCYTOPENIA 1 (disorder)
THROMBOCYTOPENIA 1 (disorder) 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.800 1.000 17 1995 2017
dbSNP: rs782290433
rs782290433 		0.882 0.120 X 48684373 missense variant G/A snv 5.5E-06
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 13 1995 2017
dbSNP: rs782290433
rs782290433 		0.882 0.120 X 48684373 missense variant G/A snv 5.5E-06
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
Neutropenia, Severe Congenital, X-Linked 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 1.000 13 1995 2017
dbSNP: rs1557006239
rs1557006239 		0.882 0.120 X 48683944 missense variant G/A snv
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 10 1995 2017
dbSNP: rs1557006239
rs1557006239 		0.882 0.120 X 48683944 missense variant G/A snv
CUI: C1839163
Disease: THROMBOCYTOPENIA 1 (disorder)
THROMBOCYTOPENIA 1 (disorder) 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 1.000 10 1995 2017
dbSNP: rs1557006239
rs1557006239 		0.882 0.120 X 48683944 missense variant G/A snv
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
Neutropenia, Severe Congenital, X-Linked 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 1.000 10 1995 2017
dbSNP: rs132630268
rs132630268 		0.882 0.120 X 48684407 missense variant G/A;C;T snv
CUI: C1839163
Disease: THROMBOCYTOPENIA 1 (disorder)
THROMBOCYTOPENIA 1 (disorder) 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 1.000 9 1997 2013
dbSNP: rs132630268
rs132630268 		0.882 0.120 X 48684407 missense variant G/A;C;T snv
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
Neutropenia, Severe Congenital, X-Linked 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 1.000 9 1997 2013
dbSNP: rs1557007123
rs1557007123 		0.882 0.120 X 48688689 stop gained C/T snv
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 6 1995 2015
dbSNP: rs1557007123
rs1557007123 		0.882 0.120 X 48688689 stop gained C/T snv
CUI: C1839163
Disease: THROMBOCYTOPENIA 1 (disorder)
THROMBOCYTOPENIA 1 (disorder) 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 1.000 6 1995 2015
dbSNP: rs1557007123
rs1557007123 		0.882 0.120 X 48688689 stop gained C/T snv
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
Neutropenia, Severe Congenital, X-Linked 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 1.000 6 1995 2015
dbSNP: rs1569493877
rs1569493877 		0.882 0.120 X 48686957 splice donor variant T/A snv
CUI: C1839163
Disease: THROMBOCYTOPENIA 1 (disorder)
THROMBOCYTOPENIA 1 (disorder) 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 1.000 2 2004 2015
dbSNP: rs1569493877
rs1569493877 		0.882 0.120 X 48686957 splice donor variant T/A snv
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 2 2004 2015
dbSNP: rs1569493877
rs1569493877 		0.882 0.120 X 48686957 splice donor variant T/A snv
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
Neutropenia, Severe Congenital, X-Linked 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 1.000 2 2004 2015
dbSNP: rs1569494025
rs1569494025 		0.882 0.120 X 48688724 frameshift variant G/- delins
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
Neutropenia, Severe Congenital, X-Linked 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 1.000 2 1996 2002
dbSNP: rs1569494025
rs1569494025 		0.882 0.120 X 48688724 frameshift variant G/- delins
CUI: C1839163
Disease: THROMBOCYTOPENIA 1 (disorder)
THROMBOCYTOPENIA 1 (disorder) 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.700 1.000 2 1996 2002
dbSNP: rs1569494025
rs1569494025 		0.882 0.120 X 48688724 frameshift variant G/- delins
CUI: C0043194
Disease: Wiskott-Aldrich Syndrome
Wiskott-Aldrich Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Immune System Diseases; Hemic and Lymphatic Diseases 0.700 1.000 2 1996 2002
dbSNP: rs132630274
rs132630274 		0.882 0.120 X 48688331 missense variant T/C snv
CUI: C1845987
Disease: Neutropenia, Severe Congenital, X-Linked
Neutropenia, Severe Congenital, X-Linked 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Hemic and Lymphatic Diseases 0.810 1.000 1 2001 2001