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.
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
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
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
222 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
49 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
11 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
1168 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
705 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
2897 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
18 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
75 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
Tuberculosis
CUI: C0041296
Disease: Tuberculosis
328 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2014 2014
Type 2 diabetes mellitus in obese
CUI: C0271638
Disease: Type 2 diabetes mellitus in obese
4 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2017 2017
Vascular Diseases
CUI: C0042373
Disease: Vascular Diseases
40 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2016 2016
Venous Thromboembolism
CUI: C1861172
Disease: Venous Thromboembolism
408 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2018 2018
Wheezing
CUI: C0043144
Disease: Wheezing
54 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2016 2016
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
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