rs9939609, FTO

N. diseases: 74
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.
Adenoma
CUI: C0001430
Disease: Adenoma
73 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.020 1.000 2 2011 2012
Age at menarche
CUI: C1314691
Disease: Age at menarche
251 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.800 1 2010 2010
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
323 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.020 1.000 2 2011 2015
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1062 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2011 2011
Aortic Valve Stenosis
CUI: C0003507
Disease: Aortic Valve Stenosis
10 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2016 2016
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
121 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.020 1.000 2 2012 2016
Asthma
CUI: C0004096
Disease: Asthma
729 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2016 2016
Atherosclerosis
CUI: C0004153
Disease: Atherosclerosis
131 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.020 1.000 2 2012 2016
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
216 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.700 1 2016 2016
Body mass index
CUI: C1305855
Disease: Body mass index
1022 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.800 6 2007 2016
Breast Carcinoma
CUI: C0678222
Disease: Breast Carcinoma
1839 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2016 2016
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
159 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2012 2012
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
197 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.070 1.000 7 2010 2016
Cerebrovascular accident
CUI: C0038454
Disease: Cerebrovascular accident
331 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.710 2 2013 2016
Colorectal Cancer
CUI: C1527249
Disease: Colorectal Cancer
955 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2012 2012
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
539 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2012 2012
Completed Suicide
CUI: C0852733
Disease: Completed Suicide
7 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2015 2015
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
760 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.810 1.000 3 2011 2016
Dementia
CUI: C0497327
Disease: Dementia
107 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2011 2011
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
143 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.020 0.500 2 2014 2016
Diabetes
CUI: C0011847
Disease: Diabetes
349 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.100 0.900 10 2009 2018
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
440 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.800 0.900 11 2009 2018
Diabetes Mellitus, Insulin-Dependent
775 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2015 2015
Diabetes Mellitus, Non-Insulin-Dependent
1522 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.900 0.938 38 2007 2016
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
256 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.700 1 2016 2016