Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
Diabetes Mellitus, Non-Insulin-Dependent
0.900 0.961 45 2007 2019
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.820 1.000 2 2011 2016
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0028754
Disease: Obesity
Obesity
0.800 0.947 149 2007 2020
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0011847
Disease: Diabetes
Diabetes
0.800 1.000 12 2010 2019
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.800 1.000 12 2010 2019
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.790 0.900 9 2009 2018
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.710 1.000 1 2013 2016
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.100 0.944 18 2008 2018
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.100 0.750 12 2009 2018
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0007222
Disease: Cardiovascular Diseases
Cardiovascular Diseases
0.080 1.000 8 2010 2018
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.070 0.857 7 2009 2018
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.070 1.000 7 2013 2018
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
0.060 0.833 6 2012 2019
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.040 0.500 4 2010 2013
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.040 0.750 4 2013 2017
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.040 0.750 4 2013 2017
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0344315
Disease: Depressed mood
Depressed mood
0.030 0.667 3 2013 2017
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0001973
Disease: Alcoholic Intoxication, Chronic
Alcoholic Intoxication, Chronic
0.030 1.000 3 2011 2014
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0346647
Disease: Malignant neoplasm of pancreas
Malignant neoplasm of pancreas
0.030 0.667 3 2012 2017
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0011570
Disease: Mental Depression
Mental Depression
0.030 0.667 3 2013 2017
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
0.030 0.667 3 2013 2017
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0235974
Disease: Pancreatic carcinoma
Pancreatic carcinoma
0.030 0.667 3 2012 2017
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0001430
Disease: Adenoma
Adenoma
0.020 1.000 2 2011 2012
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0041327
Disease: Tuberculosis, Pulmonary
Tuberculosis, Pulmonary
0.020 1.000 2 2014 2017
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0003850
Disease: Arteriosclerosis
Arteriosclerosis
0.020 1.000 2 2011 2015