Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs696217 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs641738 0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs35761398 0.701 0.520 1 23875429 missense variant TT/CC mnv 19
rs659366 0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs2501432 0.716 0.480 1 23875430 missense variant T/C;G snv 0.62 16
rs2285053 0.752 0.320 16 55478465 intron variant C/T snv 0.12 15