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.
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.050 0.800 5 2012 2018
Osteoporosis
CUI: C0029456
Disease: Osteoporosis
182 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.040 1.000 4 2015 2018
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.020 1.000 2 2010 2018
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
1082 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.020 1.000 2 2014 2015
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
1168 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.020 1.000 2 2014 2015
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.010 1.000 1 2017 2017
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.010 1.000 1 2018 2018
Malignant neoplasm of colon and/or rectum
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
502 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.010 1.000 1 2010 2010
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
1641 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.010 1.000 1 2019 2019
Neoplasms
CUI: C0027651
Disease: Neoplasms
1644 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.010 1.000 1 2016 2016
Obesity
CUI: C0028754
Disease: Obesity
1111 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.010 1.000 1 2018 2018
Polyp of large intestine
CUI: C0949059
Disease: Polyp of large intestine
32 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.010 1.000 1 2010 2010
Primary malignant neoplasm
CUI: C1306459
Disease: Primary malignant neoplasm
1374 0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 0.010 1.000 1 2019 2019