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.
Obesity
CUI: C0028754
Disease: Obesity
811 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.800 0.952 86 2008 2018
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
Overweight
CUI: C0497406
Disease: Overweight
126 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.100 0.833 12 2010 2015
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
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
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
Metabolic Syndrome X
CUI: C0524620
Disease: Metabolic Syndrome X
293 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.070 1.000 7 2008 2015
Polycystic Ovary Syndrome
CUI: C0032460
Disease: Polycystic Ovary Syndrome
181 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.070 0.714 7 2010 2017
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
Finding of body mass index
CUI: C0578022
Disease: Finding of body mass index
1022 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.800 6 2007 2016
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
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
447 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.030 0.333 3 2010 2015
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
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
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
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
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
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
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
136 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.020 0.500 2 2012 2013
Malignant Neoplasms
CUI: C0006826
Disease: Malignant Neoplasms
87 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.710 1.000 2 2016 2018
Mental Depression
CUI: C0011570
Disease: Mental Depression
137 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.020 0.500 2 2014 2016
Obesity, Morbid
CUI: C0028756
Disease: Obesity, Morbid
29 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.020 1.000 2 2012 2014
Pancreatic carcinoma
CUI: C0235974
Disease: Pancreatic carcinoma
225 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.020 0.500 2 2012 2013
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
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