rs8192284, IL6R

N. diseases: 19
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.
Rheumatoid Arthritis
CUI: C0003873
Disease: Rheumatoid Arthritis
2387 0.724 0.720 1 154454494 missense variant A/C;T snv 0.730 1.000 4 2010 2012
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.724 0.720 1 154454494 missense variant A/C;T snv 0.020 1.000 2 2007 2009
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.724 0.720 1 154454494 missense variant A/C;T snv 0.020 1.000 2 2007 2009
Fibrinogen assay
CUI: C0337428
Disease: Fibrinogen assay
143 0.724 0.720 1 154454494 missense variant A/C;T snv 0.700 1.000 2 2009 2017
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
591 0.724 0.720 1 154454494 missense variant A/C;T snv 0.020 1.000 2 2012 2020
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2012 2012
C-reactive protein measurement
CUI: C0201657
Disease: C-reactive protein measurement
624 0.724 0.720 1 154454494 missense variant A/C;T snv 0.700 1.000 1 2008 2008
Delirium
CUI: C0011206
Disease: Delirium
7 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1 2011 2011
Dengue Fever
CUI: C0011311
Disease: Dengue Fever
39 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2019 2019
Dyslipidemias
CUI: C0242339
Disease: Dyslipidemias
184 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2011 2011
Hematologic Neoplasms
CUI: C0376545
Disease: Hematologic Neoplasms
60 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2013 2013
Ischemic stroke
CUI: C0948008
Disease: Ischemic stroke
704 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2020 2020
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2014 2014
melanoma
CUI: C0025202
Disease: melanoma
515 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2008 2008
Multiple Myeloma
CUI: C0026764
Disease: Multiple Myeloma
865 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2016 2016
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2011 2011
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2014 2014
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2012 2012
Trichohepatoenteric Syndrome
CUI: C1857276
Disease: Trichohepatoenteric Syndrome
28 0.724 0.720 1 154454494 missense variant A/C;T snv 0.010 1.000 1 2010 2010