Source: BEFREE

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: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 1.000 2 2013 2017
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.020 1.000 2 2014 2015
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.020 1.000 2 2014 2015
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.020 1.000 2 2011 2018
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0022578
Disease: Keratoconus
Keratoconus 		0.020 1.000 2 2008 2013
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0021390
Disease: Inflammatory Bowel Diseases
Inflammatory Bowel Diseases 		0.010 1.000 1 2017 2017
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0036690
Disease: Septicemia
Septicemia 		0.010 < 0.001 1 2014 2014
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0003857
Disease: Congenital arteriovenous malformation
Congenital arteriovenous malformation 		0.010 1.000 1 2018 2018
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0008707
Disease: Chronic osteomyelitis
Chronic osteomyelitis 		0.010 1.000 1 2019 2019
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C1609538
Disease: Latent Tuberculosis
Latent Tuberculosis 		0.010 1.000 1 2019 2019
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
Infection caused by Helicobacter pylori 		0.010 1.000 1 2018 2018
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0011195
Disease: Dejerine-Sottas Disease (disorder)
Dejerine-Sottas Disease (disorder) 		0.010 1.000 1 2014 2014
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0009324
Disease: Ulcerative Colitis
Ulcerative Colitis 		0.010 1.000 1 2019 2019
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C4317171
Disease: Adolescent Obesity
Adolescent Obesity 		0.010 1.000 1 2016 2016
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 < 0.001 1 2018 2018
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.010 1.000 1 2010 2010
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 < 0.001 1 2018 2018
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0026691
Disease: Mucocutaneous Lymph Node Syndrome
Mucocutaneous Lymph Node Syndrome 		0.010 < 0.001 1 2019 2019
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0011311
Disease: Dengue Fever
Dengue Fever 		0.010 1.000 1 2014 2014
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0031090
Disease: Periodontal Diseases
Periodontal Diseases 		0.010 < 0.001 1 2017 2017
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C1302547
Disease: Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma
Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma 		0.010 1.000 1 2015 2015
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.010 1.000 1 2009 2009
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2019 2019
dbSNP: rs1143627
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56
CUI: C0376620
Disease: Pouchitis
Pouchitis 		0.010 1.000 1 2019 2019