Source: GWASDB

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
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.900 0.961 6 2007 2019
dbSNP: rs8050136
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.900 0.964 5 2007 2019
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C0028754
Disease: Obesity
Obesity 		0.900 1.000 4 2007 2019
dbSNP: rs8050136
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40
CUI: C0028754
Disease: Obesity
Obesity 		0.900 1.000 2 2007 2019
dbSNP: rs17817449
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv
CUI: C0028754
Disease: Obesity
Obesity 		0.890 1.000 2 2007 2016
dbSNP: rs1121980
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv
CUI: C0028754
Disease: Obesity
Obesity 		0.840 1.000 3 2007 2012
dbSNP: rs1558902
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31
CUI: C0028754
Disease: Obesity
Obesity 		0.820 0.833 4 2008 2013
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 1 2011 2016
dbSNP: rs11642841
rs11642841
FTO
0.925 0.120 16 53811575 intron variant C/A;G snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.810 1.000 3 2010 2014
dbSNP: rs7185735
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv
CUI: C0028754
Disease: Obesity
Obesity 		0.810 1.000 3 2011 2019
dbSNP: rs8043757
rs8043757
FTO
0.925 0.120 16 53779538 intron variant A/T snv 0.40
CUI: C0028754
Disease: Obesity
Obesity 		0.810 1.000 3 2011 2015
dbSNP: rs9941349
rs9941349
FTO
1.000 0.080 16 53791576 intron variant C/T snv 0.34
CUI: C0028754
Disease: Obesity
Obesity 		0.810 1.000 3 2009 2017
dbSNP: rs9936385
rs9936385
FTO
0.925 0.120 16 53785257 intron variant T/C snv 0.41
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 1.000 2 2012 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 2 2007 2020
dbSNP: rs1121980
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv
CUI: C0202236
Disease: Triglycerides measurement
Triglycerides measurement 		0.800 1.000 1 2013 2013
dbSNP: rs1121980
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv
CUI: C0392885
Disease: High density lipoprotein measurement
High density lipoprotein measurement 		0.800 1.000 1 2013 2017
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.800 1.000 1 2009 2019
dbSNP: rs1558902
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31
CUI: C0455829
Disease: Waist Circumference
Waist Circumference 		0.800 1.000 1 2009 2017
dbSNP: rs16953002
rs16953002
FTO
0.882 0.080 16 54080912 intron variant G/A snv 0.19
CUI: C0025202
Disease: melanoma
melanoma 		0.800 1.000 1 2013 2017
dbSNP: rs6499640
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs7185735
rs7185735
FTO
0.925 0.120 16 53788739 intron variant A/G;T snv
CUI: C0011860
Disease: Diabetes Mellitus, Non-Insulin-Dependent
Diabetes Mellitus, Non-Insulin-Dependent 		0.800 1.000 1 2011 2018
dbSNP: rs8050136
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40
CUI: C1305855
Disease: Body mass index
Body mass index 		0.800 1.000 1 2009 2019
dbSNP: rs8050136
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40
CUI: C0005910
Disease: Body Weight
Body Weight 		0.800 1.000 1 2009 2009
dbSNP: rs9939609
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41
CUI: C1314691
Disease: Age at menarche
Age at menarche 		0.800 1.000 1 2010 2010
dbSNP: rs9940128
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X 		0.800 1.000 1 2012 2012