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.
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.090 1.000 9 2001 2019
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
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
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
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.030 1.000 3 2005 2014
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
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.030 1.000 3 2014 2019
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.030 1.000 3 2012 2019
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
Aplastic Anemia
CUI: C0002874
Disease: Aplastic Anemia
30 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2005 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
2793 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2004 2017
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
Clear-cell metastatic renal cell carcinoma
CUI: C2931852
Disease: Clear-cell metastatic renal cell carcinoma
11 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2015 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2018 2018
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2001 2019
Ewings sarcoma
CUI: C0553580
Disease: Ewings sarcoma
25 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2012 2013
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
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2004 2017
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
277 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2012 2018
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
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2018 2019
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.020 1.000 2 2018 2019
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
Acute leukemia
CUI: C0085669
Disease: Acute leukemia
50 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.010 1.000 1 2019 2019