Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 43
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 25
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 23
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 19
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 16
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 16
rs6857 0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 15
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 14
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 11
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 10
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 8
rs9368222 1.000 0.080 6 20686765 intron variant C/A;T snv 8
rs11651052 0.851 0.200 17 37742390 intron variant G/A snv 0.50 7
rs12454712 0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 7
rs3751812
FTO
0.882 0.160 16 53784548 intron variant G/T snv 0.30 7
rs7607980 1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
rs11708067 0.882 0.080 3 123346931 intron variant A/G snv 0.19 6
rs17817964
FTO
0.925 0.120 16 53794154 intron variant C/T snv 0.30 6