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: 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: 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: 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: 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: 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: C4551761
Disease: Excessive daytime sleepiness
Excessive daytime sleepiness 		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: C0678222
Disease: Breast Carcinoma
Breast 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: C0007115
Disease: Malignant neoplasm of thyroid
Malignant neoplasm of thyroid 		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: 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: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		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: 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: 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: C0266929
Disease: Chronic Periodontitis
Chronic Periodontitis 		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: C4048328
Disease: cervical cancer
cervical cancer 		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: C0011334
Disease: Dental caries
Dental caries 		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: 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: C0376620
Disease: Pouchitis
Pouchitis 		0.010 1.000 1 2019 2019
dbSNP: rs1143629
rs1143629
IL1B
0.882 0.160 2 112835941 intron variant G/A snv 0.60
CUI: C0019196
Disease: Hepatitis C
Hepatitis C 		0.010 1.000 1 2019 2019
dbSNP: rs1143630
rs1143630
IL1B
0.827 0.160 2 112834078 intron variant T/A;G snv
CUI: C0007847
Disease: Malignant tumor of cervix
Malignant tumor of cervix 		0.010 1.000 1 2019 2019