rs2066845, NOD2

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.
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
7 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
428 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
Bacterascites
CUI: C2363867
Disease: Bacterascites
2 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
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
243 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2009 2009
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1 2010 2010
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2007 2007
Erythema Nodosum
CUI: C0014743
Disease: Erythema Nodosum
3 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2007 2007
Gastritis
CUI: C0017152
Disease: Gastritis
21 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
Gastrointestinal Crohn's disease
CUI: C1301260
Disease: Gastrointestinal Crohn's disease
2 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2015 2015
Guillain-Barre Syndrome
CUI: C0018378
Disease: Guillain-Barre Syndrome
13 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
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
139 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2009 2009
Hepatitis B
CUI: C0019163
Disease: Hepatitis B
519 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2019 2019
Hirschsprung Disease
CUI: C0019569
Disease: Hirschsprung Disease
162 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
Ileal Diseases
CUI: C0020875
Disease: Ileal Diseases
7 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2002 2002
INFLAMMATORY BOWEL DISEASE 5
CUI: C1853438
Disease: INFLAMMATORY BOWEL DISEASE 5
2 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
Intestinal Diseases
CUI: C0021831
Disease: Intestinal Diseases
13 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
Malignant neoplasm of stomach
CUI: C0024623
Disease: Malignant neoplasm of stomach
615 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2013 2013
Rectal Carcinoma
CUI: C0007113
Disease: Rectal Carcinoma
112 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2008 2008
Spondylarthropathies
CUI: C0949691
Disease: Spondylarthropathies
7 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2005 2005
Stomach Carcinoma
CUI: C0699791
Disease: Stomach Carcinoma
652 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2013 2013
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