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: rs1477196
rs1477196
FTO
0.851 0.200 16 53774346 intron variant A/G snv 0.71
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms
0.020 < 0.001 2 2013 2017
dbSNP: rs1477196
rs1477196
FTO
0.851 0.200 16 53774346 intron variant A/G snv 0.71
CUI: C1306459
Disease: Primary malignant neoplasm
Primary malignant neoplasm
0.020 < 0.001 2 2013 2017
dbSNP: rs11642015
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31
CUI: C0028754
Disease: Obesity
Obesity
0.010 < 0.001 1 2014 2014
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
0.010 < 0.001 1 2014 2014
dbSNP: rs1558902
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31
Diabetes Mellitus, Non-Insulin-Dependent
0.010 < 0.001 1 2016 2016
dbSNP: rs1558902
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease
0.010 < 0.001 1 2010 2010
dbSNP: rs17817449
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv
CUI: C2362324
Disease: Pediatric Obesity
Pediatric Obesity
0.010 < 0.001 1 2014 2014
dbSNP: rs9921255
rs9921255
FTO
1.000 0.080 16 53975416 intron variant T/C snv 0.20
CUI: C0028754
Disease: Obesity
Obesity
0.010 < 0.001 1 2012 2012
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0086543
Disease: Cataract
Cataract
0.010 < 0.001 1 2019 2019
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C1956346
Disease: Coronary Artery Disease
Coronary Artery Disease
0.010 < 0.001 1 2016 2016
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder
0.010 < 0.001 1 2016 2016
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0342546
Disease: Premature adrenarche
Premature adrenarche
0.010 < 0.001 1 2009 2009
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C0342257
Disease: Complications of Diabetes Mellitus
Complications of Diabetes Mellitus
0.010 < 0.001 1 2012 2012
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: rs1121980
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv
CUI: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.020 0.500 2 2013 2015
dbSNP: rs1121980
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast
0.020 0.500 2 2013 2015
dbSNP: rs62048402
rs62048402
FTO
0.882 0.200 16 53769311 intron variant G/A snv 0.31
CUI: C0028754
Disease: Obesity
Obesity
0.020 0.500 2 2014 2014
dbSNP: rs8044769
rs8044769
FTO
0.851 0.200 16 53805223 intron variant T/A;C;G snv
CUI: C0029408
Disease: Degenerative polyarthritis
Degenerative polyarthritis
0.030 0.667 3 2014 2018
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: 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: 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: 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: 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: 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: C0678222
Disease: Breast Carcinoma
Breast Carcinoma
0.040 0.750 4 2013 2017