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 Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1 2016 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
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
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
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
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
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
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
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
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2011 2011
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
81 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2011 2011
Latent Autoimmune Diabetes in Adults
12 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2019 2019
Latent autoimmune diabetes mellitus in adult
12 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2019 2019
Major Depressive Disorder
CUI: C1269683
Disease: Major Depressive Disorder
1451 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1 2016 2016
Malignant Childhood Neoplasm
CUI: C0278704
Disease: Malignant Childhood Neoplasm
34 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2018 2018
Malignant Pleural Mesothelioma
CUI: C0812413
Disease: Malignant Pleural Mesothelioma
15 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2018 2018
Metabolic Diseases
CUI: C0025517
Disease: Metabolic Diseases
50 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2018 2018
Miscarriage
CUI: C4552766
Disease: Miscarriage
56 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2015 2015
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
680 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2009 2009