IL18, interleukin 18, 3606

N. diseases: 750; N. variants: 18
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1834481
rs1834481 		0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16
CUI: C2697766
Disease: Interleukin 18 Measurement
Interleukin 18 Measurement 		0.800 1.000 1 2010 2010
dbSNP: rs1834481
rs1834481 		0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2014 2014
dbSNP: rs5744256
rs5744256 		0.827 0.120 11 112152125 intron variant A/G snv 0.16
CUI: C0201657
Disease: C-reactive protein measurement
C-reactive protein measurement 		0.700 1.000 1 2014 2014
dbSNP: rs1946518
rs1946518 		0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.050 1.000 5 2011 2020
dbSNP: rs549908
rs549908 		0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.050 1.000 5 2003 2019
dbSNP: rs187238
rs187238 		0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		Nutritional and Metabolic Diseases; Immune System Diseases; Endocrine System Diseases 0.030 1.000 3 2013 2017
dbSNP: rs187238
rs187238 		0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.030 0.333 3 2012 2015
dbSNP: rs187238
rs187238 		0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.030 0.333 3 2005 2014
dbSNP: rs187238
rs187238 		0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.030 1.000 3 2015 2019
dbSNP: rs1946518
rs1946518 		0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		Skin and Connective Tissue Diseases; Musculoskeletal Diseases; Immune System Diseases 0.030 0.333 3 2005 2014
dbSNP: rs1946518
rs1946518 		0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.030 0.333 3 2016 2019
dbSNP: rs1946518
rs1946518 		0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.030 0.667 3 2012 2015
dbSNP: rs360719
rs360719 		0.790 0.480 11 112165426 non coding transcript exon variant A/G snv 0.25
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.030 1.000 3 2011 2015
dbSNP: rs549908
rs549908 		0.752 0.440 11 112150193 synonymous variant T/A;G snv 4.2E-06; 0.29
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		Skin and Connective Tissue Diseases; Immune System Diseases 0.030 1.000 3 2009 2019
dbSNP: rs187238
rs187238 		0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		Digestive System Diseases; Infections 0.020 1.000 2 2009 2019
dbSNP: rs187238
rs187238 		0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		Infections 0.020 1.000 2 2019 2020
dbSNP: rs187238
rs187238 		0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		Digestive System Diseases; Neoplasms 0.020 0.500 2 2016 2017
dbSNP: rs187238
rs187238 		0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		Digestive System Diseases; Infections 0.020 1.000 2 2012 2019
dbSNP: rs187238
rs187238 		0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.020 1.000 2 2012 2019
dbSNP: rs187238
rs187238 		0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.020 1.000 2 2014 2015
dbSNP: rs187238
rs187238 		0.602 0.680 11 112164265 intron variant C/A;G snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.020 1.000 2 2016 2019
dbSNP: rs1946518
rs1946518 		0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		Nervous System Diseases; Cardiovascular Diseases 0.020 1.000 2 2010 2013
dbSNP: rs1946518
rs1946518 		0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0004096
Disease: Asthma
Asthma 		Respiratory Tract Diseases; Immune System Diseases 0.020 1.000 2 2012 2019
dbSNP: rs1946518
rs1946518 		0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		Digestive System Diseases 0.020 1.000 2 2014 2018
dbSNP: rs1946518
rs1946518 		0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		Digestive System Diseases 0.020 1.000 2 2015 2018