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.
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
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
59 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
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
Latent Autoimmune Diabetes in Adults
CUI: C1739108
Disease: Latent Autoimmune Diabetes in Adults
8 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
CUI: C1960272
Disease: 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
362 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
20 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
547 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2009 2009
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
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
189 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
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
Pregnancy associated hypertension
CUI: C0852036
Disease: Pregnancy associated hypertension
43 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2016 2016
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
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
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
Psoriasis
CUI: C0033860
Disease: Psoriasis
238 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2019 2019
Schizophrenia
CUI: C0036341
Disease: Schizophrenia
1332 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
Sleep Apnea Syndromes
CUI: C0037315
Disease: Sleep Apnea Syndromes
5 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2019 2019
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
67 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014