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: rs1143629
rs1143629
IL1B
0.882 0.160 2 112835941 intron variant G/A snv 0.60
CUI: C1279420
Disease: Anxiety neurosis (finding)
Anxiety neurosis (finding) 		0.010 1.000 1 2017 2017
dbSNP: rs1143629
rs1143629
IL1B
0.882 0.160 2 112835941 intron variant G/A snv 0.60
CUI: C0700613
Disease: Anxiety state
Anxiety state 		0.010 1.000 1 2017 2017
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
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: C0302592
Disease: Cervix carcinoma
Cervix carcinoma 		0.010 1.000 1 2019 2019
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: 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: 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: C2239176
Disease: Liver carcinoma
Liver 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: 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: 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: 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: 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: 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: 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: 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: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach 		0.010 1.000 1 2018 2018
dbSNP: rs1143642
rs1143642
IL1B
2 112830976 intron variant A/G snv 0.89
CUI: C4531177
Disease: Sleep onset Insomnia
Sleep onset Insomnia 		0.010 1.000 1 2015 2015
dbSNP: rs1143643
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29
CUI: C0086132
Disease: Depressive Symptoms
Depressive Symptoms 		0.010 1.000 1 2016 2016
dbSNP: rs1143643
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29
CUI: C0339143
Disease: Thyroid associated opthalmopathies
Thyroid associated opthalmopathies 		0.010 1.000 1 2010 2010
dbSNP: rs1143643
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29
CUI: C0860603
Disease: Anxiety symptoms
Anxiety symptoms 		0.010 1.000 1 2016 2016
dbSNP: rs1143643
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
Secondary malignant neoplasm of lymph node 		0.010 1.000 1 2012 2012
dbSNP: rs1143643
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29
CUI: C0243026
Disease: Sepsis
Sepsis 		0.010 1.000 1 2014 2014
dbSNP: rs1143643
rs1143643
IL1B
0.790 0.320 2 112830725 intron variant C/T snv 0.29
CUI: C0343641
Disease: Human papilloma virus infection
Human papilloma virus infection 		0.010 1.000 1 2016 2016