Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.100 1.000 14 2009 2019
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.100 0.923 13 2009 2019
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.090 1.000 9 2012 2019
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.070 1.000 7 2012 2018
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.060 1.000 6 2009 2019
dbSNP: rs17300539
rs17300539 		0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.060 0.833 6 2011 2019
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.060 0.833 6 2008 2017
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.060 1.000 6 2010 2017
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes 		Nutritional and Metabolic Diseases; Female Urogenital Diseases and Pregnancy Complications; Endocrine System Diseases 0.060 1.000 6 2010 2019
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.060 0.833 6 2011 2019
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.050 0.800 5 2011 2019
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.050 0.600 5 2011 2018
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.050 0.800 5 2013 2015
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.050 0.800 5 2013 2015
dbSNP: rs16861194
rs16861194 		0.925 0.120 3 186841636 upstream gene variant A/G snv 0.15
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.050 0.800 5 2009 2018
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0028754
Disease: Obesity
Obesity 		Pathological Conditions, Signs and Symptoms; Nutritional and Metabolic Diseases 0.050 1.000 5 2013 2020
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.040 0.750 4 2014 2015
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.040 1.000 4 2015 2019
dbSNP: rs1501299
rs1501299 		0.597 0.720 3 186853334 intron variant G/C;T snv
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		Nutritional and Metabolic Diseases 0.040 1.000 4 2011 2018
dbSNP: rs182052
rs182052 		0.701 0.440 3 186842993 intron variant G/A snv 0.38
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		Nutritional and Metabolic Diseases; Endocrine System Diseases 0.040 1.000 4 2009 2019
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		Neoplasms 0.040 0.500 4 2013 2017
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.040 0.750 4 2008 2017
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm 		Neoplasms 0.040 0.500 4 2013 2017
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		Cardiovascular Diseases 0.040 1.000 4 2010 2017
dbSNP: rs266729
rs266729 		0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.040 1.000 4 2015 2020