Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs12979860 0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs4938723 0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2070744 0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs187238 0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs2853676 0.667 0.560 5 1288432 intron variant T/A;C snv 29
rs12255372 0.667 0.480 10 113049143 intron variant G/A;T snv 28
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs11066280 0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs12785878 0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24