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.
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
CUI: C4722085
Disease: 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
Periodontitis
CUI: C0031099
Disease: Periodontitis
116 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2013 2013
Sacroiliitis
CUI: C0574960
Disease: Sacroiliitis
2 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2013 2013
Salivary Gland Pleomorphic Adenoma
CUI: C1519176
Disease: Salivary Gland Pleomorphic Adenoma
9 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2008 2008
Sarcoidosis
CUI: C0036202
Disease: Sarcoidosis
787 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2011 2011
Sjogren's Syndrome
CUI: C1527336
Disease: Sjogren's Syndrome
47 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2009 2009
Spondylarthritis
CUI: C0949690
Disease: Spondylarthritis
23 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2013 2013
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1 2015 2015
Superficial ulcer
CUI: C0333307
Disease: Superficial ulcer
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
Systemic Scleroderma
CUI: C0036421
Disease: Systemic Scleroderma
287 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2009 2009
Thyroid associated opthalmopathies
CUI: C0339143
Disease: Thyroid associated opthalmopathies
49 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1 2008 2008
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2012 2012
Uveitis
CUI: C0042164
Disease: Uveitis
43 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 1.000 1 2011 2011