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
Diabetes Mellitus, Non-Insulin-Dependent
2672 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.040 1.000 4 2004 2019
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
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
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
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.800 1.000 3 2008 2019
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
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.850 0.889 9 2010 2019
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
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.030 0.667 3 2011 2020
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
Asthma
CUI: C0004096
Disease: Asthma
1536 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.040 1.000 4 2012 2017
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
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
Aortic Aneurysm, Abdominal
CUI: C0162871
Disease: Aortic Aneurysm, Abdominal
90 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.020 1.000 2 2013 2019
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
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
Eczema
CUI: C0013595
Disease: Eczema
368 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 0.710 1.000 2 2013 2019
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