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
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.860 0.800 10 2007 2019
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.850 0.818 11 2008 2019
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
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.060 1.000 6 2010 2018
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.050 1.000 5 2010 2017
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.810 1.000 3 2010 2019
Asthma
CUI: C0004096
Disease: Asthma
1536 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.020 1.000 2 2010 2016
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2010 2010
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
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
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
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.700 1.000 1 2011 2011
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
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
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
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
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
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
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
Kidney Failure, Chronic
CUI: C0022661
Disease: Kidney Failure, Chronic
425 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2014 2014
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
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.030 0.667 3 2015 2018
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.020 1.000 2 2015 2018