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: rs6499640
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59
CUI: C0028754
Disease: Obesity
Obesity
0.020 1.000 2 2011 2014
dbSNP: rs6499640
rs6499640
FTO
0.925 0.160 16 53735765 intron variant G/A snv 0.59
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease
0.010 1.000 1 2012 2012
dbSNP: rs62048379
rs62048379
FTO
1.000 0.080 16 53763271 intron variant C/A snv 8.4E-02
CUI: C0028754
Disease: Obesity
Obesity
0.010 1.000 1 2017 2017
dbSNP: rs7206790
rs7206790
FTO
0.925 0.160 16 53763996 intron variant C/G snv 0.49
CUI: C0028754
Disease: Obesity
Obesity
0.710 1.000 1 2011 2014
dbSNP: rs9937053
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 1.000 1 2011 2011
dbSNP: rs9937053
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42
CUI: C0007787
Disease: Transient Ischemic Attack
Transient Ischemic Attack
0.010 1.000 1 2011 2011
dbSNP: rs9937053
rs9937053
FTO
0.882 0.160 16 53765595 intron variant G/A snv 0.42
CUI: C0917805
Disease: Transient Cerebral Ischemia
Transient Cerebral Ischemia
0.010 1.000 1 2011 2011
dbSNP: rs9928094
rs9928094
FTO
1.000 0.080 16 53765993 intron variant A/G snv 0.42
CUI: C0028754
Disease: Obesity
Obesity
0.710 1.000 1 2011 2013
dbSNP: rs9930333
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv
CUI: C0028754
Disease: Obesity
Obesity
0.710 1.000 1 2011 2013
dbSNP: rs9940128
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42
Diabetes Mellitus, Non-Insulin-Dependent
0.010 1.000 1 2011 2011
dbSNP: rs9940128
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42
CUI: C4529962
Disease: Fatty Liver Disease
Fatty Liver Disease
0.010 1.000 1 2017 2017
dbSNP: rs9940128
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42
CUI: C0028754
Disease: Obesity
Obesity
0.710 1.000 1 2007 2012
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 18 2007 2019
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C0524620
Disease: Metabolic Syndrome X
Metabolic Syndrome X
0.030 1.000 3 2011 2018
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C0032460
Disease: Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
0.030 1.000 3 2008 2019
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
Diabetes Mellitus, Non-Insulin-Dependent
0.730 1.000 3 2009 2019
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C0011849
Disease: Diabetes Mellitus
Diabetes Mellitus
0.020 1.000 2 2010 2017
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C0085207
Disease: Gestational Diabetes
Gestational Diabetes
0.020 1.000 2 2017 2018
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C0011847
Disease: Diabetes
Diabetes
0.020 1.000 2 2010 2017
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: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C1281440
Disease: Familial obesity
Familial obesity
0.010 1.000 1 2009 2009
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C0027794
Disease: Neural Tube Defects
Neural Tube Defects
0.010 1.000 1 2012 2012
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C0038454
Disease: Cerebrovascular accident
Cerebrovascular accident
0.010 1.000 1 2013 2013
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C2937224
Disease: Constitutional obesity
Constitutional obesity
0.010 1.000 1 2009 2009
dbSNP: rs1421085
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31
CUI: C0242339
Disease: Dyslipidemias
Dyslipidemias
0.010 1.000 1 2014 2014