rs2066842, NOD2

N. diseases: 15
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 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.790 1.000 9 2002 2014
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
392 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.040 0.750 4 2002 2014
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.020 1.000 2 2008 2014
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1441 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.020 1.000 2 2010 2014
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.020 1.000 2 2010 2014
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.010 1.000 1 2010 2010
Ileal Diseases
CUI: C0020875
Disease: Ileal Diseases
7 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.010 1.000 1 2012 2012
Infection caused by Helicobacter pylori
CUI: C0850666
Disease: Infection caused by Helicobacter pylori
56 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.010 1.000 1 2010 2010
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
277 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.010 1.000 1 2002 2002
Intestinal metaplasia
CUI: C0334037
Disease: Intestinal metaplasia
24 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.010 1.000 1 2010 2010
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.010 1.000 1 2008 2008
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
751 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.010 1.000 1 2013 2013
PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
CUI: C1868675
Disease: PARKINSON DISEASE 2, AUTOSOMAL RECESSIVE JUVENILE
11 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.010 1.000 1 2013 2013
Spondylarthritis
CUI: C0949690
Disease: Spondylarthritis
23 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.010 1.000 1 2002 2002
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.763 0.200 16 50710713 missense variant C/A;T snv 4.0E-06; 0.19 0.010 1.000 1 2013 2013