rs1946518, IL18

N. diseases: 46
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.
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.050 1.000 5 2011 2020
Liver carcinoma
CUI: C2239176
Disease: Liver carcinoma
942 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.030 0.333 3 2016 2019
Lupus Erythematosus, Systemic
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
1172 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.030 0.667 3 2012 2015
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.030 0.333 3 2005 2014
Asthma
CUI: C0004096
Disease: Asthma
1536 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.020 1.000 2 2012 2019
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.020 1.000 2 2015 2018
Diabetes Mellitus, Insulin-Dependent
954 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.020 1.000 2 2013 2015
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.020 1.000 2 2012 2019
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.020 1.000 2 2009 2019
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.020 1.000 2 2010 2013
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.020 1.000 2 2014 2018
Active tuberculosis
CUI: C0151332
Disease: Active tuberculosis
25 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2019 2019
Acute monocytic leukemia
CUI: C0023465
Disease: Acute monocytic leukemia
22 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2017 2017
Adult Lymphoma
CUI: C1332206
Disease: Adult Lymphoma
66 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2017 2017
Alopecia
CUI: C0002170
Disease: Alopecia
375 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2018 2018
Alopecia Areata
CUI: C0002171
Disease: Alopecia Areata
54 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2018 2018
Alzheimer Disease, Late Onset
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
243 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2009 2009
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2009 2009
Anxiety
CUI: C0003467
Disease: Anxiety
287 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2017 2017
Anxiety Disorders
CUI: C0003469
Disease: Anxiety Disorders
163 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2017 2017
Biliary Atresia
CUI: C0005411
Disease: Biliary Atresia
32 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2018 2018
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2015 2015
Chagas Disease
CUI: C0041234
Disease: Chagas Disease
10 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2019 2019
Childhood Lymphoma
CUI: C1332979
Disease: Childhood Lymphoma
66 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2017 2017
Congenital atresia of extrahepatic bile duct
19 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2018 2018