rs2228145, IL6R

N. diseases: 57
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.
INTERLEUKIN 6, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
1 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.700 0
SOLUBLE INTERLEUKIN-6 RECEPTOR, SERUM LEVEL OF, QUANTITATIVE TRAIT LOCUS
1 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.700 0
Obesity
CUI: C0028754
Disease: Obesity
1111 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.040 0.750 4 2004 2007
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2007 2007
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2007 2007
Trichohepatoenteric Syndrome
CUI: C1857276
Disease: Trichohepatoenteric Syndrome
28 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2010 2010
Fatigue
CUI: C0015672
Disease: Fatigue
67 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2011 2011
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2012 2012
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.020 1.000 2 2013 2013
Diabetes Mellitus, Insulin-Dependent
954 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.020 1.000 2 2012 2013
fibrinogen activity
CUI: C1325327
Disease: fibrinogen activity
63 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.700 1.000 2 2009 2013
Fibrinogen assay
CUI: C0337428
Disease: Fibrinogen assay
143 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.700 1.000 2 2009 2013
Fibrinogen, CTCAE
CUI: C1561955
Disease: Fibrinogen, CTCAE
63 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.700 1.000 2 2009 2013
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.020 1.000 2 2006 2013
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2013 2013
Henoch-Schoenlein Purpura
CUI: C0034152
Disease: Henoch-Schoenlein Purpura
59 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1 2013 2013
Mastocytosis
CUI: C0024899
Disease: Mastocytosis
8 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2013 2013
Aortic Valve Stenosis
CUI: C0003507
Disease: Aortic Valve Stenosis
19 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2014 2014
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2014 2014
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2014 2014
Congenital contractural arachnodactyly
48 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2014 2014
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2014 2014
Dermatitis, Atopic
CUI: C0011615
Disease: Dermatitis, Atopic
232 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.710 1.000 2 2013 2015
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
2897 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2015 2015
Dementia
CUI: C0497327
Disease: Dementia
176 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.010 1.000 1 2016 2016