Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0041296
Disease: Tuberculosis
Tuberculosis 		0.050 1.000 5 2011 2020
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis 		0.030 0.333 3 2005 2014
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0024141
Disease: Lupus Erythematosus, Systemic
Lupus Erythematosus, Systemic 		0.030 0.667 3 2012 2015
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.030 0.333 3 2016 2019
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0019163
Disease: Hepatitis B
Hepatitis B 		0.020 1.000 2 2012 2019
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.020 1.000 2 2013 2015
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0948008
Disease: Ischemic stroke
Ischemic stroke 		0.020 1.000 2 2010 2013
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.020 1.000 2 2014 2018
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0004096
Disease: Asthma
Asthma 		0.020 1.000 2 2012 2019
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.020 1.000 2 2015 2018
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.020 1.000 2 2009 2019
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0003467
Disease: Anxiety
Anxiety 		0.010 1.000 1 2017 2017
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid 		0.010 1.000 1 2015 2015
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C1096197
Disease: Immune reconstitution syndrome
Immune reconstitution syndrome 		0.010 1.000 1 2013 2013
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0005411
Disease: Biliary Atresia
Biliary Atresia 		0.010 1.000 1 2018 2018
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0151332
Disease: Active tuberculosis
Active tuberculosis 		0.010 1.000 1 2019 2019
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.010 1.000 1 2013 2013
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
Leukemia, Myelocytic, Acute 		0.010 1.000 1 2017 2017
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0494463
Disease: Alzheimer Disease, Late Onset
Alzheimer Disease, Late Onset 		0.010 1.000 1 2009 2009
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2011 2011
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0278996
Disease: Malignant Head and Neck Neoplasm
Malignant Head and Neck Neoplasm 		0.010 1.000 1 2018 2018
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C4520983
Disease: Congenital atresia of extrahepatic bile duct
Congenital atresia of extrahepatic bile duct 		0.010 1.000 1 2018 2018
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		0.010 1.000 1 2017 2017
dbSNP: rs1946518
rs1946518
IL18
0.602 0.760 11 112164735 intron variant T/G snv 0.60
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		0.010 1.000 1 2017 2017