rs9939609, FTO

N. diseases: 98
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.
Coronary heart disease
CUI: C0010068
Disease: Coronary heart disease
1178 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.820 1.000 4 2011 2016
Dementia
CUI: C0497327
Disease: Dementia
176 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2011 2011
Depressed mood
CUI: C0344315
Disease: Depressed mood
269 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.030 0.667 3 2013 2017
Depressive disorder
CUI: C0011581
Disease: Depressive disorder
297 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.030 0.667 3 2013 2017
Diabetes
CUI: C0011847
Disease: Diabetes
710 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.800 1.000 13 2010 2019
Diabetes Mellitus
CUI: C0011849
Disease: Diabetes Mellitus
824 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.800 1.000 13 2010 2019
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
954 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
Diabetes Mellitus, Non-Insulin-Dependent
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
2672 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.900 0.961 51 2007 2019
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016
Eating Disorders
CUI: C0013473
Disease: Eating Disorders
42 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2012 2012
elevated blood glucose level
CUI: C0495706
Disease: elevated blood glucose level
111 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
326 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.020 1.000 2 2011 2017
Fatty Liver Disease
CUI: C4529962
Disease: Fatty Liver Disease
81 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2017 2017
Finding of body mass index
CUI: C0578022
Disease: Finding of body mass index
252 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 4 2007 2013
Gestational Diabetes
CUI: C0085207
Disease: Gestational Diabetes
224 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.070 1.000 7 2013 2018
Glucose measurement
CUI: C0337438
Disease: Glucose measurement
111 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016
Heart failure
CUI: C0018801
Disease: Heart failure
201 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
347 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016
Human immunodeficiency virus (HIV) II infection category B1
CUI: C3854222
Disease: Human immunodeficiency virus (HIV) II infection category B1
56 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
Hunger
CUI: C0020175
Disease: Hunger
12 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2009 2009
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
108 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.020 1.000 2 2008 2018
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
64 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
1085 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.040 0.500 4 2010 2013