rs11209026, IL23R

N. diseases: 46
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.
Acquired aplastic anemia
CUI: C0271907
Disease: Acquired aplastic anemia
12 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1 2009 2009
Acute GVH disease
CUI: C0856825
Disease: Acute GVH disease
49 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2008 2008
Acute pancreatitis
CUI: C0001339
Disease: Acute pancreatitis
51 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2019 2019
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
609 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.900 1.000 14 2008 2018
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2015 2015
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
89 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.040 1.000 4 2008 2019
Arthropathy
CUI: C0022408
Disease: Arthropathy
10 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2013 2013
Asthma
CUI: C0004096
Disease: Asthma
1536 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.020 1.000 2 2015 2016
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
281 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2015 2015
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
428 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.020 1.000 2 2011 2011
Barrett Esophagus
CUI: C0004763
Disease: Barrett Esophagus
60 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2008 2008
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2014 2014
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2008 2008
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2015 2015
Complete atrioventricular block
CUI: C0151517
Disease: Complete atrioventricular block
96 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2017 2017
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
1147 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.900 0.944 36 2006 2020
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1 2013 2013
Eclampsia
CUI: C0013537
Disease: Eclampsia
38 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2019 2019
Genital ulcers
CUI: C0151281
Disease: Genital ulcers
6 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2014 2014
Granulomatosis, Orofacial
CUI: C0399496
Disease: Granulomatosis, Orofacial
3 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2016 2016
Graves Disease
CUI: C0018213
Disease: Graves Disease
352 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1 2008 2008
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1 2015 2015
Idiopathic achalasia of esophagus
CUI: C0859976
Disease: Idiopathic achalasia of esophagus
2 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2010 2010
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
605 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.900 0.773 22 2006 2020
Inflammatory disorder
CUI: C1290884
Disease: Inflammatory disorder
8 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2011 2011