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.
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
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
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2015 2015
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
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
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
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2019 2019
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
3417 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2017 2017
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2020 2020
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
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
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
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
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 0.010 1.000 1 2015 2015
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