rs9939609, FTO

N. diseases: 80
Source: BEFREE ×
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.
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
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
547 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2009 2009
Premature adrenarche
CUI: C0342546
Disease: Premature adrenarche
6 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1 2009 2009
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
858 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2010 2010
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
968 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2011 2011
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
355 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2011 2011
Dementia
CUI: C0497327
Disease: Dementia
165 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2011 2011
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
223 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
80 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2011 2011
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2011 2011
Adenoma
CUI: C0001430
Disease: Adenoma
103 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.020 1.000 2 2011 2012
Anorexia Nervosa
CUI: C0003125
Disease: Anorexia Nervosa
52 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2012 2012
Bulimia Nervosa
CUI: C2267227
Disease: Bulimia Nervosa
21 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2012 2012
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
1186 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2012 2012
Complications of Diabetes Mellitus
CUI: C0342257
Disease: Complications of Diabetes Mellitus
35 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1 2012 2012
Eating Disorders
CUI: C0013473
Disease: Eating Disorders
33 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2012 2012
Neural Tube Defects
CUI: C0027794
Disease: Neural Tube Defects
122 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2012 2012
Obesity, Morbid
CUI: C0028756
Disease: Obesity, Morbid
48 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2012 2012
Hypertensive disease
CUI: C0020538
Disease: Hypertensive disease
871 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.040 0.500 4 2010 2013
Alcoholic Intoxication, Chronic
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
223 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.030 1.000 3 2011 2014
Completed Suicide
CUI: C0852733
Disease: Completed Suicide
33 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
Diabetes Mellitus, Insulin-Dependent
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
388 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
Hepatitis C
CUI: C0019196
Disease: Hepatitis C
316 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
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
Hyperinsulinism
CUI: C0020459
Disease: Hyperinsulinism
59 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014