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
956 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.900 0.917 40 2007 2016
Inflammatory Bowel Disease 10
CUI: C1970207
Disease: Inflammatory Bowel Disease 10
1 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.700 11 2004 2016
Ulcerative Colitis
CUI: C0009324
Disease: Ulcerative Colitis
696 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.090 0.778 9 2007 2010
Inflammatory Bowel Diseases
CUI: C0021390
Disease: Inflammatory Bowel Diseases
451 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.050 1.000 5 2008 2010
Ileal Diseases
CUI: C0020875
Disease: Ileal Diseases
6 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.020 1.000 2 2008 2009
Colon Carcinoma
CUI: C0699790
Disease: Colon Carcinoma
240 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2016 2016
Colonic Diseases
CUI: C0009373
Disease: Colonic Diseases
4 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2008 2008
Colorectal Cancer
CUI: C1527249
Disease: Colorectal Cancer
955 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2016 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
539 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2016 2016
Hamartoma Syndrome, Multiple
CUI: C0018553
Disease: Hamartoma Syndrome, Multiple
46 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2010 2010
Huntington Disease
CUI: C0020179
Disease: Huntington Disease
68 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2010 2010
Infection caused by Helicobacter pylori
53 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2016 2016
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
36 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2008 2008
Malignant neoplasm of thyroid
CUI: C0007115
Disease: Malignant neoplasm of thyroid
40 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2016 2016
Malignant tumor of colon
CUI: C0007102
Disease: Malignant tumor of colon
135 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2016 2016
Metastatic malignant neoplasm to brain
17 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2018 2018
Necrotizing Enterocolitis
CUI: C0520459
Disease: Necrotizing Enterocolitis
3 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2017 2017
Necrotizing enterocolitis in fetus OR newborn
10 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2017 2017
Non-Small Cell Lung Carcinoma
CUI: C0007131
Disease: Non-Small Cell Lung Carcinoma
362 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2018 2018
Obesity
CUI: C0028754
Disease: Obesity
811 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2015 2015
Osteitis Deformans
CUI: C0029401
Disease: Osteitis Deformans
48 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2016 2016
Pediatric Crohn's disease
CUI: C2931133
Disease: Pediatric Crohn's disease
3 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2014 2014
Thyroid carcinoma
CUI: C0549473
Disease: Thyroid carcinoma
81 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2016 2016
Ulcer
CUI: C0041582
Disease: Ulcer
10 0.662 0.393 2 233274722 missense variant A/G snp 0.45 0.43 0.010 1.000 1 2016 2016