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.
BORNHOLM EYE DISEASE
CUI: C3159311
Disease: BORNHOLM EYE DISEASE
1 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2019 2019
Cataract
CUI: C0086543
Disease: Cataract
124 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1 2019 2019
Latent Autoimmune Diabetes in Adults
12 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
12 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2019 2019
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
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
Affective Symptoms
CUI: C0001726
Disease: Affective Symptoms
10 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2018 2018
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
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
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
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
Asthma
CUI: C0004096
Disease: Asthma
1536 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2016 2016
Atrial Fibrillation
CUI: C0004238
Disease: Atrial Fibrillation
584 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016
Coronary Artery Disease
CUI: C1956346
Disease: Coronary Artery Disease
1577 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1 2016 2016
Diastolic blood pressure
CUI: C0428883
Disease: Diastolic blood pressure
1037 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016
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
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
High density lipoprotein measurement
1440 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016
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
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
Serum total cholesterol measurement
CUI: C1445957
Disease: Serum total cholesterol measurement
1243 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.700 1.000 1 2016 2016