rs2066845, NOD2

N. diseases: 43
Source: BEFREE ×
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.
Crohn Disease
CUI: C0010346
Disease: Crohn Disease
456 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 1.000 0.949 69 2001 2019
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
392 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.800 0.846 12 2002 2018
Ankylosing spondylitis
CUI: C0038013
Disease: Ankylosing spondylitis
273 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.730 0.750 3 2002 2016
Psoriasis
CUI: C0033860
Disease: Psoriasis
238 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.710 1.000 1 2006 2016
SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES (disorder)
10 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.710 1.000 1 2003 2011
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
277 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.100 1.000 11 2002 2017
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.060 0.833 6 2005 2014
Malignant neoplasm of colon and/or rectum
502 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.040 0.750 4 2005 2008
Sarcoidosis
CUI: C0036202
Disease: Sarcoidosis
65 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.040 0.750 4 2005 2018
Arthritis, Psoriatic
CUI: C0003872
Disease: Arthritis, Psoriatic
50 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.030 1.000 3 2004 2010
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.030 1.000 3 2003 2018
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.030 0.667 3 2005 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.030 0.667 3 2005 2014
Bronchiolitis Obliterans
CUI: C0006272
Disease: Bronchiolitis Obliterans
5 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.020 1.000 2 2008 2019
Primary bacterial peritonitis
CUI: C0275551
Disease: Primary bacterial peritonitis
11 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.020 1.000 2 2012 2016
Sepsis
CUI: C0243026
Disease: Sepsis
139 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.020 1.000 2 2007 2012
Septicemia
CUI: C0036690
Disease: Septicemia
139 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.020 1.000 2 2007 2012
Spondylarthritis
CUI: C0949690
Disease: Spondylarthritis
23 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.020 1.000 2 2002 2005
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
306 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.020 1.000 2 2012 2013
Acute Inflammatory Demyelinating Polyneuropathy
2 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2016 2016
Acute Motor Axonal Neuropathy
CUI: C3890941
Disease: Acute Motor Axonal Neuropathy
4 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2016 2016
Acute motor sensory axonal neuropathy
2 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2016 2016
Aggressive periodontitis, generalized
16 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2006 2006
Ascites
CUI: C0003962
Disease: Ascites
5 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2012 2012
Autoimmune Diseases
CUI: C0004364
Disease: Autoimmune Diseases
213 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2010 2010