rs1800795, IL6;LOC541472

N. diseases: 58
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.
Diabetes
CUI: C0011847
Disease: Diabetes
349 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2006 2006
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
440 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2006 2006
Glioma
CUI: C0017638
Disease: Glioma
180 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2008 2008
Kidney Diseases
CUI: C0022658
Disease: Kidney Diseases
93 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2009 2009
Retinal Diseases
CUI: C0035309
Disease: Retinal Diseases
35 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2009 2009
Degenerative polyarthritis
CUI: C0029408
Disease: Degenerative polyarthritis
92 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.020 1.000 2 2008 2010
Adenoma of large intestine
CUI: C1302401
Disease: Adenoma of large intestine
61 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2010 2010
Osteoarthritis of hip
CUI: C0029410
Disease: Osteoarthritis of hip
26 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2010 2010
Cerebral Palsy
CUI: C0007789
Disease: Cerebral Palsy
17 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2011 2011
Diabetes Mellitus, Non-Insulin-Dependent
1522 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.030 1.000 3 2006 2012
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
447 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.020 1.000 2 2009 2012
Acute GVH disease
CUI: C0856825
Disease: Acute GVH disease
19 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2012 2012
Dementia, Vascular
CUI: C0011269
Disease: Dementia, Vascular
15 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2012 2012
Obesity
CUI: C0028754
Disease: Obesity
811 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2012 2012
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
1839 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.040 1.000 4 2007 2013
Malignant neoplasm of breast
CUI: C0006142
Disease: Malignant neoplasm of breast
1365 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.040 1.000 4 2007 2013
Fatigue
CUI: C0015672
Disease: Fatigue
33 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.020 1.000 2 2012 2013
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
149 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2013 2013
Central neuroblastoma
CUI: C0700095
Disease: Central neuroblastoma
87 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.020 1.000 2 2009 2014
Neuroblastoma
CUI: C0027819
Disease: Neuroblastoma
288 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.020 1.000 2 2009 2014
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
121 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2014 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
131 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2014 2014
Classical Hodgkin's Lymphoma
CUI: C1333064
Disease: Classical Hodgkin's Lymphoma
17 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2014 2014
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
1782 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.010 1.000 1 2014 2014
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
341 0.580 0.607 7 22727026 intron variant C/G snp 0.68 0.030 1.000 3 2013 2015