rs1143643, IL1B

N. diseases: 10
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Anxiety symptoms
CUI: C0860603
Disease: Anxiety symptoms
10 0.790 0.320 2 112830725 intron variant C/T snv 0.29 0.010 1.000 1 2016 2016
Deep caries
CUI: C0333523
Disease: Deep caries
1 0.790 0.320 2 112830725 intron variant C/T snv 0.29 0.010 1.000 1 2015 2015
Depressive Symptoms
CUI: C0086132
Disease: Depressive Symptoms
120 0.790 0.320 2 112830725 intron variant C/T snv 0.29 0.010 1.000 1 2016 2016
Human papilloma virus infection
CUI: C0343641
Disease: Human papilloma virus infection
42 0.790 0.320 2 112830725 intron variant C/T snv 0.29 0.010 1.000 1 2016 2016
Papillary thyroid carcinoma
CUI: C0238463
Disease: Papillary thyroid carcinoma
204 0.790 0.320 2 112830725 intron variant C/T snv 0.29 0.010 1.000 1 2012 2012
Secondary malignant neoplasm of lymph node
CUI: C0686619
Disease: Secondary malignant neoplasm of lymph node
188 0.790 0.320 2 112830725 intron variant C/T snv 0.29 0.010 1.000 1 2012 2012
Sepsis
CUI: C0243026
Disease: Sepsis
144 0.790 0.320 2 112830725 intron variant C/T snv 0.29 0.010 1.000 1 2014 2014
Septicemia
CUI: C0036690
Disease: Septicemia
141 0.790 0.320 2 112830725 intron variant C/T snv 0.29 0.010 1.000 1 2014 2014
Stress, Psychological
CUI: C0038443
Disease: Stress, Psychological
24 0.790 0.320 2 112830725 intron variant C/T snv 0.29 0.010 1.000 1 2016 2016
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.790 0.320 2 112830725 intron variant C/T snv 0.29 0.010 1.000 1 2010 2010