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: rs1043973338
rs1043973338
IL1B
0.882 0.080 2 112830483 missense variant A/C snv
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2007 2007
dbSNP: rs1043973338
rs1043973338
IL1B
0.882 0.080 2 112830483 missense variant A/C snv
CUI: C0242379
Disease: Malignant neoplasm of lung
Malignant neoplasm of lung 		0.010 1.000 1 2007 2007
dbSNP: rs1043973338
rs1043973338
IL1B
0.882 0.080 2 112830483 missense variant A/C snv
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2007 2007
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: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2018 2018
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0027498
Disease: Nausea and vomiting
Nausea and vomiting 		0.010 1.000 1 2019 2019
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0020651
Disease: Hypotension, Orthostatic
Hypotension, Orthostatic 		0.010 1.000 1 2019 2019
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2011 2011
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0021122
Disease: Disruptive, Impulse Control, and Conduct Disorders
Disruptive, Impulse Control, and Conduct Disorders 		0.010 1.000 1 2019 2019
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		0.010 1.000 1 2019 2019
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0007134
Disease: Renal Cell Carcinoma
Renal Cell Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0279702
Disease: Conventional (Clear Cell) Renal Cell Carcinoma
Conventional (Clear Cell) Renal Cell Carcinoma 		0.010 1.000 1 2017 2017
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2016 2016
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C1306460
Disease: Primary malignant neoplasm of lung
Primary malignant neoplasm of lung 		0.010 1.000 1 2018 2018
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0028754
Disease: Obesity
Obesity 		0.010 1.000 1 2015 2015
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0855247
Disease: Sleep attack
Sleep attack 		0.010 1.000 1 2019 2019
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
Non-Small Cell Lung Carcinoma 		0.010 1.000 1 2015 2015
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0007113
Disease: Rectal Carcinoma
Rectal Carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0040136
Disease: Thyroid Neoplasm
Thyroid Neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		0.010 1.000 1 2019 2019
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2011 2011
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.010 1.000 1 2019 2019
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		0.010 1.000 1 2019 2019
dbSNP: rs1143623
rs1143623
IL1B
0.677 0.440 2 112838252 upstream gene variant C/G snv 0.24
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2014 2014