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: 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: 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: C0684249
Disease: Carcinoma of lung
Carcinoma of lung 		0.010 1.000 1 2007 2007
dbSNP: rs1143630
rs1143630
IL1B
0.827 0.160 2 112834078 intron variant T/A;G snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2011 2011
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
dbSNP: rs1143630
rs1143630
IL1B
0.827 0.160 2 112834078 intron variant T/A;G snv
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
Secondary malignant neoplasm of lymph node 		0.010 1.000 1 2012 2012
dbSNP: rs1143630
rs1143630
IL1B
0.827 0.160 2 112834078 intron variant T/A;G snv
CUI: C4048328
Disease: cervical cancer
cervical cancer 		0.010 1.000 1 2019 2019
dbSNP: rs1143630
rs1143630
IL1B
0.827 0.160 2 112834078 intron variant T/A;G snv
CUI: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2019 2019
dbSNP: rs1143633
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv
CUI: C1527304
Disease: Allergic Reaction
Allergic Reaction 		0.700 1.000 1 2017 2017
dbSNP: rs1143633
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis 		0.010 1.000 1 2007 2007
dbSNP: rs1143633
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv
CUI: C0270736
Disease: Essential Tremor
Essential Tremor 		0.010 1.000 1 2019 2019
dbSNP: rs1143633
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv
CUI: C0038436
Disease: Post-Traumatic Stress Disorder
Post-Traumatic Stress Disorder 		0.010 1.000 1 2017 2017
dbSNP: rs1143633
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv
CUI: C0238463
Disease: Papillary thyroid carcinoma
Papillary thyroid carcinoma 		0.010 1.000 1 2012 2012
dbSNP: rs1143633
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2018 2018
dbSNP: rs1143633
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs1143633
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv
CUI: C0035258
Disease: Restless Legs Syndrome
Restless Legs Syndrome 		0.010 1.000 1 2014 2014
dbSNP: rs1143633
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
Secondary malignant neoplasm of lymph node 		0.010 1.000 1 2012 2012
dbSNP: rs1143633
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		0.010 1.000 1 2011 2011
dbSNP: rs1143633
rs1143633
IL1B
0.752 0.280 2 112832890 intron variant C/G;T snv
CUI: C2239176
Disease: Liver carcinoma
Liver carcinoma 		0.010 1.000 1 2018 2018
dbSNP: rs3087258
rs3087258
IL1B
0.925 0.080 2 112837294 upstream gene variant G/A snv
CUI: C0011265
Disease: Presenile dementia
Presenile dementia 		0.010 1.000 1 2012 2012
dbSNP: rs3087258
rs3087258
IL1B
0.925 0.080 2 112837294 upstream gene variant G/A snv
CUI: C0497327
Disease: Dementia
Dementia 		0.010 1.000 1 2012 2012
dbSNP: rs549858786
rs549858786
IL1B
0.790 0.320 2 112836807 5 prime UTR variant T/A snv
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		0.010 1.000 1 2015 2015
dbSNP: rs549858786
rs549858786
IL1B
0.790 0.320 2 112836807 5 prime UTR variant T/A snv
CUI: C0008533
Disease: Hemophilia B
Hemophilia B 		0.010 1.000 1 2015 2015
dbSNP: rs549858786
rs549858786
IL1B
0.790 0.320 2 112836807 5 prime UTR variant T/A snv
CUI: C0033860
Disease: Psoriasis
Psoriasis 		0.010 1.000 1 2015 2015
dbSNP: rs549858786
rs549858786
IL1B
0.790 0.320 2 112836807 5 prime UTR variant T/A snv
CUI: C0024530
Disease: Malaria
Malaria 		0.010 1.000 1 2015 2015