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.
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
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
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
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
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
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
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
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
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
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
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