UCP2, uncoupling protein 2, 7351

N. diseases: 235; N. variants: 5
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: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C4237343
Disease: Overweight or obesity
Overweight or obesity 		0.010 1.000 1 2018 2018
dbSNP: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C1960636
Disease: Dysglycemia
Dysglycemia 		0.010 1.000 1 2013 2013
dbSNP: rs778724159
rs778724159 		0.925 0.080 11 73978066 missense variant C/T snv 1.6E-05 7.0E-06
CUI: C4722085
Disease: Malignant neoplasm of colon and/or rectum
Malignant neoplasm of colon and/or rectum 		0.010 1.000 1 2013 2013
dbSNP: rs659366
rs659366 		0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40
CUI: C1843898
Disease: BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 (disorder)
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 (disorder) 		0.700 0
dbSNP: rs659366
rs659366 		0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs659366
rs659366 		0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40
CUI: C0948089
Disease: Acute Coronary Syndrome
Acute Coronary Syndrome 		Cardiovascular Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs659366
rs659366 		0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
Premature coronary artery atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs659366
rs659366 		0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
Premature coronary artery atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2019 2019
dbSNP: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2008 2008
dbSNP: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C0004153
Disease: Atherosclerosis
Atherosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2008 2008
dbSNP: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C0010054
Disease: Coronary Arteriosclerosis
Coronary Arteriosclerosis 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease 		Cardiovascular Diseases 0.010 1.000 1 2013 2013
dbSNP: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs659366
rs659366 		0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40
CUI: C0742343
Disease: Acute Chest Syndrome
Acute Chest Syndrome 		Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Respiratory Tract Diseases; Hemic and Lymphatic Diseases 0.010 < 0.001 1 2016 2016
dbSNP: rs659366
rs659366 		0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
Non-alcoholic Fatty Liver Disease 		Digestive System Diseases 0.010 1.000 1 2017 2017
dbSNP: rs659366
rs659366 		0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs778724159
rs778724159 		0.925 0.080 11 73978066 missense variant C/T snv 1.6E-05 7.0E-06
CUI: C0009402
Disease: Colorectal Carcinoma
Colorectal Carcinoma 		Digestive System Diseases; Neoplasms 0.010 1.000 1 2013 2013
dbSNP: rs659366
rs659366 		0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.030 1.000 3 2010 2017
dbSNP: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C0011847
Disease: Diabetes
Diabetes 		Endocrine System Diseases 0.030 1.000 3 2008 2016
dbSNP: rs659366
rs659366 		0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.010 1.000 1 2018 2018
dbSNP: rs660339
rs660339 		0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43
CUI: C0011884
Disease: Diabetic Retinopathy
Diabetic Retinopathy 		Eye Diseases; Endocrine System Diseases; Cardiovascular Diseases 0.010 1.000 1 2012 2012