rs4251961, IL1RN

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.
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.763 0.200 2 113116890 intron variant T/C snv 0.29 0.010 1.000 1 2018 2018
Coronary Arteriosclerosis
CUI: C0010054
Disease: Coronary Arteriosclerosis
440 0.763 0.200 2 113116890 intron variant T/C snv 0.29 0.010 1.000 1 2014 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.763 0.200 2 113116890 intron variant T/C snv 0.29 0.010 1.000 1 2014 2014
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.763 0.200 2 113116890 intron variant T/C snv 0.29 0.010 1.000 1 2014 2014
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.763 0.200 2 113116890 intron variant T/C snv 0.29 0.010 1.000 1 2014 2014
Fatigue
CUI: C0015672
Disease: Fatigue
67 0.763 0.200 2 113116890 intron variant T/C snv 0.29 0.010 1.000 1 2015 2015
Invasive Streptococcus pneumoniae disease
CUI: C1320214
Disease: Invasive Streptococcus pneumoniae disease
9 0.763 0.200 2 113116890 intron variant T/C snv 0.29 0.010 1.000 1 2011 2011
Pneumonia
CUI: C0032285
Disease: Pneumonia
33 0.763 0.200 2 113116890 intron variant T/C snv 0.29 0.010 1.000 1 2014 2014
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.763 0.200 2 113116890 intron variant T/C snv 0.29 0.010 1.000 1 2016 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
827 0.763 0.200 2 113116890 intron variant T/C snv 0.29 0.010 1.000 1 2014 2014