rs9939609, FTO

N. diseases: 74
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.
Waist-Hip Ratio
CUI: C0205682
Disease: Waist-Hip Ratio
320 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.700 1 2008 2008
heart rate
CUI: C0018810
Disease: heart rate
75 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.700 1 2009 2009
Hyperglycemia
CUI: C0020456
Disease: Hyperglycemia
37 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2009 2009
Premature adrenarche
CUI: C0342546
Disease: Premature adrenarche
3 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1 2009 2009
Waist Circumference
CUI: C0455829
Disease: Waist Circumference
227 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.700 1 2009 2009
Age at menarche
CUI: C1314691
Disease: Age at menarche
251 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.800 1 2010 2010
Hunger
CUI: C0020175
Disease: Hunger
8 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2010 2010
Myocardial Infarction
CUI: C0027051
Disease: Myocardial Infarction
454 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2010 2010
Smoking Behaviors
CUI: C1519383
Disease: Smoking Behaviors
753 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.700 1 2010 2010
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1062 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2011 2011
Dementia
CUI: C0497327
Disease: Dementia
107 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2011 2011
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
121 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1 2011 2011
Malignant neoplasm of prostate
CUI: C0376358
Disease: Malignant neoplasm of prostate
563 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2011 2011
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
102 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2011 2011
Prostate carcinoma
CUI: C0600139
Disease: Prostate carcinoma
756 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2011 2011
Adenoma
CUI: C0001430
Disease: Adenoma
73 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.020 1.000 2 2011 2012
Carcinogenesis
CUI: C0596263
Disease: Carcinogenesis
159 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2012 2012
Colorectal Cancer
CUI: C1527249
Disease: Colorectal Cancer
955 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2012 2012
Colorectal Carcinoma
CUI: C0009402
Disease: Colorectal Carcinoma
539 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2012 2012
Endometrial Carcinoma
CUI: C0476089
Disease: Endometrial Carcinoma
145 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2012 2012
Impaired glucose tolerance
CUI: C0271650
Disease: Impaired glucose tolerance
55 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2012 2012
Malignant neoplasm of endometrium
CUI: C0007103
Disease: Malignant neoplasm of endometrium
106 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2012 2012
Pediatric Obesity
CUI: C2362324
Disease: Pediatric Obesity
31 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2012 2012
Uterine Corpus Cancer
CUI: C1883486
Disease: Uterine Corpus Cancer
106 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.010 1.000 1 2012 2012
Malignant neoplasm of pancreas
CUI: C0346647
Disease: Malignant neoplasm of pancreas
136 0.580 0.607 16 53786615 intron variant T/A snp 0.42 0.020 0.500 2 2012 2013