rs231775, CTLA4

N. diseases: 115
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Bullous Dermatitis
CUI: C0085932
Disease: Bullous Dermatitis
1 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2000 2000
Bullous pemphigoid
CUI: C0030805
Disease: Bullous pemphigoid
11 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2000 2000
Pemphigoid, Benign Mucous Membrane
CUI: C0030804
Disease: Pemphigoid, Benign Mucous Membrane
1 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2000 2000
Disorder of eye
CUI: C0015397
Disease: Disorder of eye
14 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2003 2003
Adrenoleukodystrophy
CUI: C0162309
Disease: Adrenoleukodystrophy
116 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2004 2004
Alcoholic Liver Diseases
CUI: C0023896
Disease: Alcoholic Liver Diseases
20 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2004 2004
Immunosuppression
CUI: C4048329
Disease: Immunosuppression
9 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2005 2005
Thromboangiitis Obliterans
CUI: C0040021
Disease: Thromboangiitis Obliterans
16 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1 2005 2005
Hepatitis B, Chronic
CUI: C0524909
Disease: Hepatitis B, Chronic
84 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2006 2006
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2006 2006
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
275 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2007 2007
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
688 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2007 2007
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.030 0.333 3 2003 2008
Acquired haemophilia
CUI: C1096116
Disease: Acquired haemophilia
2 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2008 2008
Hemophilia A
CUI: C0019069
Disease: Hemophilia A
295 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2008 2008
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1 2008 2008
Uveitis, Intermediate
CUI: C0042166
Disease: Uveitis, Intermediate
10 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2008 2008
Uveomeningoencephalitic Syndrome
CUI: C0042170
Disease: Uveomeningoencephalitic Syndrome
27 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2008 2008
Autoimmune thyroid disease
CUI: C0178468
Disease: Autoimmune thyroid disease
15 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.030 1.000 3 2002 2009
Acute anterior uveitis
CUI: C0701807
Disease: Acute anterior uveitis
30 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1 2009 2009
Postpartum Thyroiditis
CUI: C0271815
Disease: Postpartum Thyroiditis
1 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2009 2009
Vitiligo
CUI: C0042900
Disease: Vitiligo
249 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1 2009 2009
VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
CUI: C1847835
Disease: VITILIGO-ASSOCIATED MULTIPLE AUTOIMMUNE DISEASE SUSCEPTIBILITY 1 (finding)
92 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1 2009 2009
Carcinoma
CUI: C0007097
Disease: Carcinoma
103 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2010 2010
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2010 2010