rs3087243, CTLA4

N. diseases: 44
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.
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
1 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.700 0
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
1 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.700 0
Appendicitis
CUI: C0003615
Disease: Appendicitis
10 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2020 2020
Ewings sarcoma
CUI: C0553580
Disease: Ewings sarcoma
25 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2013 2013
Cytomegalovirus Infections
CUI: C0010823
Disease: Cytomegalovirus Infections
26 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2015 2015
Thyroid Diseases
CUI: C0040128
Disease: Thyroid Diseases
26 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2014 2014
Drug-Induced Liver Disease
CUI: C0860207
Disease: Drug-Induced Liver Disease
29 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2012 2012
SVEINSSON CHORIORETINAL ATROPHY
CUI: C1862382
Disease: SVEINSSON CHORIORETINAL ATROPHY
30 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2013 2013
Rheumatic Heart Disease
CUI: C0035439
Disease: Rheumatic Heart Disease
33 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2016 2016
Autoantibody measurement
CUI: C1272321
Disease: Autoantibody measurement
52 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.700 1.000 1 2011 2011
Autoimmune thyroid disease (AITD)
CUI: C3840565
Disease: Autoimmune thyroid disease (AITD)
54 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.030 1.000 3 2009 2014
Fatigue
CUI: C0015672
Disease: Fatigue
67 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2013 2013
Giant Cell Arteritis
CUI: C0039483
Disease: Giant Cell Arteritis
78 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2016 2016
Myasthenia Gravis
CUI: C0026896
Disease: Myasthenia Gravis
93 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.020 0.500 2 2018 2019
Immune System Diseases
CUI: C0021053
Disease: Immune System Diseases
116 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.700 1.000 1 2011 2011
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2016 2016
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
CUI: C4310768
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 2
132 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
CUI: C3150797
Disease: AUTOIMMUNE DISEASE, SUSCEPTIBILITY TO, 6
141 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.700 1.000 1 2019 2019
AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
CUI: C4014795
Disease: AUTOIMMUNE DISEASE, MULTISYSTEM, INFANTILE-ONSET, 1
142 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.700 1.000 1 2019 2019
Childhood Osteosarcoma
CUI: C1332986
Disease: Childhood Osteosarcoma
151 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2011 2011
Osteosarcoma of bone
CUI: C0585442
Disease: Osteosarcoma of bone
151 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2011 2011
Allergic rhinitis (disorder)
CUI: C2607914
Disease: Allergic rhinitis (disorder)
176 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2016 2016
Osteosarcoma
CUI: C0029463
Disease: Osteosarcoma
178 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2011 2011
Chronic kidney disease stage 5
CUI: C2316810
Disease: Chronic kidney disease stage 5
194 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2014 2014
Hypothyroidism
CUI: C0020676
Disease: Hypothyroidism
283 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.700 1.000 2 2016 2019