Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10010131 0.827 0.120 4 6291188 intron variant A/G snv 0.66 0.63 7
rs10146997 0.827 0.240 14 79478819 intron variant A/G snv 0.25 6
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10423928 0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs10767664 0.752 0.400 11 27704439 intron variant T/A snv 0.83 16
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10885406 0.925 0.120 10 113017965 intron variant A/G snv 0.55 2
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs10946398 0.827 0.160 6 20660803 intron variant A/C snv 0.40 7
rs10968576 0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs11075989
FTO
0.925 0.120 16 53785965 intron variant C/A;T snv 3
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 6
rs11196205 0.827 0.200 10 113047288 intron variant G/A;C;T snv 7
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs11642015
FTO
0.925 0.120 16 53768582 intron variant C/T snv 0.31 9
rs11642841
FTO
0.925 0.120 16 53811575 intron variant C/A;G snv 3
rs11671664 0.925 0.120 19 45669020 intron variant G/A snv 0.12 5
rs12086634 0.827 0.280 1 209706914 intron variant T/G snv 0.21 0.20 6
rs12104705 0.882 0.120 2 162435107 intron variant C/T snv 0.15 4
rs12156368 0.925 0.120 8 18885203 intron variant C/T snv 0.36 2
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs13078807 0.925 0.120 3 85835000 intron variant A/G snv 0.15 5
rs1412239 0.925 0.120 9 28425517 intron variant C/G snv 0.26 4
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28