rs659366, UCP2

N. diseases: 17
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.
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 (disorder)
CUI: C1843898
Disease: BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 (disorder)
1 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.700 0
Obesity
CUI: C0028754
Disease: Obesity
1111 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.050 0.800 5 2007 2015
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.030 1.000 3 2010 2017
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.030 1.000 3 2010 2017
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.020 0.500 2 2014 2018
Acute Chest Syndrome
CUI: C0742343
Disease: Acute Chest Syndrome
135 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1 2016 2016
Acute Coronary Syndrome
CUI: C0948089
Disease: Acute Coronary Syndrome
139 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1 2016 2016
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1962 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1.000 1 2013 2013
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1.000 1 2013 2013
Diabetic Retinopathy
CUI: C0011884
Disease: Diabetic Retinopathy
213 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1.000 1 2018 2018
Essential Hypertension
CUI: C0085580
Disease: Essential Hypertension
293 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1.000 1 2019 2019
Mood Disorders
CUI: C0525045
Disease: Mood Disorders
308 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1.000 1 2017 2017
Multiple Sclerosis
CUI: C0026769
Disease: Multiple Sclerosis
1022 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1.000 1 2009 2009
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1.000 1 2017 2017
Pediatric Obesity
CUI: C2362324
Disease: Pediatric Obesity
67 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1.000 1 2007 2007
PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
CUI: C1845050
Disease: PIGMENTARY DISORDER, RETICULATE, WITH SYSTEMIC MANIFESTATIONS
37 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1.000 1 2014 2014
Premature coronary artery atherosclerosis
CUI: C1867743
Disease: Premature coronary artery atherosclerosis
43 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.010 1.000 1 2019 2019