rs187238, IL18

N. diseases: 48
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.602 0.680 11 112164265 intron variant C/A;G snv 0.030 1.000 3 2015 2019
Diabetes Mellitus, Insulin-Dependent
954 0.602 0.680 11 112164265 intron variant C/A;G snv 0.030 1.000 3 2013 2017
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.602 0.680 11 112164265 intron variant C/A;G snv 0.030 0.333 3 2012 2015
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.602 0.680 11 112164265 intron variant C/A;G snv 0.030 0.333 3 2005 2014
Asthma
CUI: C0004096
Disease: Asthma
1536 0.602 0.680 11 112164265 intron variant C/A;G snv 0.020 1.000 2 2012 2019
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.602 0.680 11 112164265 intron variant C/A;G snv 0.020 1.000 2 2016 2019
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.602 0.680 11 112164265 intron variant C/A;G snv 0.020 1.000 2 2012 2019
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.602 0.680 11 112164265 intron variant C/A;G snv 0.020 1.000 2 2009 2019
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.602 0.680 11 112164265 intron variant C/A;G snv 0.020 0.500 2 2016 2017
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.602 0.680 11 112164265 intron variant C/A;G snv 0.020 1.000 2 2019 2020
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.602 0.680 11 112164265 intron variant C/A;G snv 0.020 1.000 2 2014 2015
Active tuberculosis
CUI: C0151332
Disease: Active tuberculosis
25 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2019 2019
Alopecia
CUI: C0002170
Disease: Alopecia
375 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2018 2018
Alopecia Areata
CUI: C0002171
Disease: Alopecia Areata
54 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2018 2018
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2009 2009
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2009 2009
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2017 2017
Biliary Atresia
CUI: C0005411
Disease: Biliary Atresia
32 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2018 2018
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2016 2016
Carotid Stenosis
CUI: C0007282
Disease: Carotid Stenosis
19 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2018 2018
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2015 2015
Colitis
CUI: C0009319
Disease: Colitis
15 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2019 2019
Congenital atresia of extrahepatic bile duct
19 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2018 2018
Conventional (Clear Cell) Renal Cell Carcinoma
222 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2010 2010
Cytomegalovirus Infections
CUI: C0010823
Disease: Cytomegalovirus Infections
26 0.602 0.680 11 112164265 intron variant C/A;G snv 0.010 1.000 1 2019 2019