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.
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.100 0.875 16 1998 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.060 0.833 6 1998 2017
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.030 0.667 3 1998 2015
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.100 0.875 16 1999 2019
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
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
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
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.100 0.900 10 2002 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
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
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
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 0.050 0.600 5 2004 2015
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
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
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
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
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
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