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: rs1445888481
rs1445888481
IL1B
0.925 0.080 2 112835572 synonymous variant C/T snv 7.0E-06
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.100 1.000 10 2002 2018
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.060 0.833 6 2006 2016
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.040 0.750 4 2010 2014
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.030 1.000 3 2013 2018
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis 		0.030 1.000 3 2014 2019
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		0.030 1.000 3 2015 2019
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: 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: 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: 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: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		0.020 1.000 2 2013 2017
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		0.020 1.000 2 2010 2011
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions 		0.020 1.000 2 2018 2018
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.020 1.000 2 2016 2017
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.020 1.000 2 2015 2019
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0015672
Disease: Fatigue
Fatigue 		0.020 0.500 2 2011 2012
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0011570
Disease: Mental Depression
Mental Depression 		0.020 1.000 2 2016 2019
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0376358
Disease: Malignant neoplasm of prostate
Malignant neoplasm of prostate 		0.020 1.000 2 2014 2015
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0022578
Disease: Keratoconus
Keratoconus 		0.020 1.000 2 2008 2013
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.020 1.000 2 2015 2019
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.020 1.000 2 2010 2013
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0243026
Disease: Sepsis
Sepsis 		0.020 0.500 2 2014 2016
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0031090
Disease: Periodontal Diseases
Periodontal Diseases 		0.020 0.500 2 2014 2019
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0036690
Disease: Septicemia
Septicemia 		0.020 0.500 2 2014 2016
dbSNP: rs16944
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57
CUI: C0600139
Disease: Prostate carcinoma
Prostate carcinoma 		0.020 1.000 2 2014 2015