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.
Anorexia Nervosa
CUI: C0003125
Disease: Anorexia Nervosa
72 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2012 2012
Steatohepatitis
CUI: C2711227
Disease: Steatohepatitis
75 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
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
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
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
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
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
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
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
Cataract
CUI: C0086543
Disease: Cataract
124 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1 2019 2019
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
Tuberculosis, Pulmonary
CUI: C0041327
Disease: Tuberculosis, Pulmonary
171 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.020 1.000 2 2014 2017
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
Waist Circumference
CUI: C0455829
Disease: Waist Circumference
183 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2009 2009
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
197 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.020 1.000 2 2011 2017
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
Non-alcoholic Fatty Liver Disease
CUI: C0400966
Disease: Non-alcoholic Fatty Liver Disease
222 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
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
Polysomnography
CUI: C0162701
Disease: Polysomnography
249 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2007 2007
Body mass index procedure
CUI: C0005893
Disease: Body mass index procedure
252 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 4 2007 2013
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
Celiac Disease
CUI: C0007570
Disease: Celiac Disease
263 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2015 2015
Arteriosclerosis
CUI: C0003850
Disease: Arteriosclerosis
267 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.020 1.000 2 2011 2015
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