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
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
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
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
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
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 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
Juvenile arthritis
CUI: C3495559
Disease: Juvenile arthritis
128 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2011 2011
Malignant neoplasm of colon and/or rectum
502 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2015 2015
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1 2015 2015
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2008 2008
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1 2008 2008
Pediatric Crohn's disease
CUI: C2931133
Disease: Pediatric Crohn's disease
6 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2007 2007