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.
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.070 0.857 7 2008 2018
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
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.050 1.000 5 2009 2018
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
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.030 1.000 3 2010 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2010 2015
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
Chronic Obstructive Airway Disease
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
852 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2010 2010
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.050 1.000 5 2011 2017
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.030 1.000 3 2011 2019
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2011 2019
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
712 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2011 2013
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2011 2019
Glioma
CUI: C0017638
Disease: Glioma
353 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2011 2011
Graft-vs-Host Disease
CUI: C0018133
Disease: Graft-vs-Host Disease
25 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2011 2011
Mucocutaneous Lymph Node Syndrome
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
195 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2011 2011