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.
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
CUI: C4520983
Disease: 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
Conventional (Clear Cell) Renal Cell Carcinoma
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
222 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2010 2010
Cytomegalovirus Infections
CUI: C0010823
Disease: Cytomegalovirus Infections
26 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2019 2019
Depressive Symptoms
CUI: C0086132
Disease: Depressive Symptoms
120 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2017 2017
Hashimoto Disease
CUI: C0677607
Disease: Hashimoto Disease
131 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1 2013 2013
Head and Neck Carcinoma
CUI: C3887461
Disease: Head and Neck Carcinoma
118 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2018 2018
IGA Glomerulonephritis
CUI: C0017661
Disease: IGA Glomerulonephritis
130 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2018 2018
Immune Reconstitution Inflammatory Syndrome
CUI: C1619738
Disease: Immune Reconstitution Inflammatory Syndrome
5 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2013 2013
Immune reconstitution syndrome
CUI: C1096197
Disease: Immune reconstitution syndrome
4 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2013 2013
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2017 2017
Liver diseases
CUI: C0023895
Disease: Liver diseases
100 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2020 2020
Lymphoma
CUI: C0024299
Disease: Lymphoma
91 0.602 0.760 11 112164735 intron variant T/G snv 0.60 0.010 1.000 1 2017 2017