Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.800 0.947 151 2007 2020
dbSNP: rs1805192
rs1805192
PPARG
121 0.510 0.840 3 12379739 missense variant C/G snv 0.100 0.837 43 1997 2018
dbSNP: rs17782313
rs17782313 		34 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 0.900 0.905 42 2008 2019
dbSNP: rs7566605
rs7566605
LOC107985940
11 0.752 0.320 2 118078449 regulatory region variant C/G snv 0.70 0.100 0.667 30 2006 2015
dbSNP: rs1421085
rs1421085
FTO
28 0.752 0.280 16 53767042 intron variant T/C snv 0.31 0.900 1.000 22 2007 2019
dbSNP: rs8050136
rs8050136
FTO
32 0.716 0.560 16 53782363 intron variant C/A snv 0.40 0.900 1.000 15 2007 2019
dbSNP: rs12970134
rs12970134 		13 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 0.100 0.923 13 2009 2019
dbSNP: rs10938397
rs10938397 		19 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 0.890 0.800 10 2010 2019
dbSNP: rs17817449
rs17817449
FTO
21 0.716 0.560 16 53779455 intron variant T/A;G snv 0.890 1.000 10 2007 2016
dbSNP: rs7903146
rs7903146
TCF7L2
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.100 0.900 10 2008 2019
dbSNP: rs7138803
rs7138803 		17 0.827 0.240 12 49853685 intergenic variant G/A;T snv 0.860 0.889 9 2011 2014
dbSNP: rs6548238
rs6548238 		10 0.882 0.200 2 634905 TF binding site variant T/C snv 0.85 0.080 1.000 8 2009 2019
dbSNP: rs7799039
rs7799039
LOC105375494
33 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 0.070 1.000 7 2008 2018
dbSNP: rs9930506
rs9930506
FTO
16 0.776 0.360 16 53796553 intron variant A/G snv 0.36 0.760 0.857 7 2008 2018
dbSNP: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.840 1.000 6 2007 2012
dbSNP: rs1256046734
rs1256046734
LEPR
12 0.763 0.280 1 65621409 missense variant A/G snv 7.0E-06 0.060 1.000 6 2009 2018
dbSNP: rs1501299
rs1501299
ADIPOQ ; ADIPOQ-AS1
52 0.597 0.720 3 186853334 intron variant G/C;T snv 0.060 1.000 6 2009 2019
dbSNP: rs1558902
rs1558902
FTO
21 0.827 0.120 16 53769662 intron variant T/A snv 0.31 0.820 0.833 6 2008 2013
dbSNP: rs2016520
rs2016520
PPARD
16 0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 0.060 1.000 6 2010 2017
dbSNP: rs266729
rs266729
ADIPOQ
37 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 0.050 1.000 5 2013 2020
dbSNP: rs659366
rs659366
UCP2
17 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 0.050 0.800 5 2007 2015
dbSNP: rs662799
rs662799
APOA5
33 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 0.050 1.000 5 2011 2015
dbSNP: rs987237
rs987237
TFAP2B
10 0.925 0.120 6 50835337 intron variant A/G snv 0.17 0.740 1.000 5 2009 2015
dbSNP: rs1527483
rs1527483
CD36
2 1.000 0.080 7 80672184 intron variant G/A snv 6.7E-02 0.040 1.000 4 2010 2018
dbSNP: rs16147
rs16147
NPY ; LOC107986777
18 0.695 0.400 7 24283791 upstream gene variant T/C snv 0.48 0.040 1.000 4 2012 2015