Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.699 0.286 2 27518370 intron variant T/C snp 0.67 20
rs2075650 0.699 0.357 19 44892362 intron variant A/G snp 0.13 0.14 16
rs964184 0.756 0.286 11 116778201 3 prime UTR variant G/C snp 0.83 13
rs1229984 0.622 0.393 4 99318162 missense variant T/C,G snp 0.90 0.94 12
rs4420638 0.724 0.321 19 44919689 intergenic variant A/G snp 0.19 12
rs671 0.593 0.464 12 111803962 missense variant G/A snp 1.9E-02 1.3E-02 10
rs8050136
FTO
0.744 0.321 16 53782363 intron variant C/A snp 0.40 10
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 10
rs12229654 0.801 0.214 12 110976657 intergenic variant T/G snp 1.1E-02 9
rs174547 0.846 0.071 11 61803311 intron variant T/C snp 0.30 8
rs1121980
FTO
0.923 0.107 16 53775335 intron variant G/A,C snp 0.44 8
rs2068834 2 27616672 intron variant T/C snp 0.28 8
rs629301 0.878 0.071 1 109275684 3 prime UTR variant G/T snp 0.75 7
rs13107325 1.000 0.036 4 102267552 missense variant C/A,T snp 4.0E-06; 4.5E-02 4.3E-02 7
rs17782313 0.734 0.250 18 60183864 intergenic variant T/C snp 0.23 6
rs7138803 0.923 0.107 12 49853685 intergenic variant G/A,T snp 0.32; 3.2E-05 6
rs1421085
FTO
0.821 0.107 16 53767042 intron variant T/C snp 0.32 6
rs9940128
FTO
0.923 0.071 16 53766842 intron variant G/A snp 0.42 6
rs10938397 0.846 0.179 4 45180510 intergenic variant A/G snp 0.38 5
rs12970134 0.878 0.107 18 60217517 intergenic variant G/A snp 0.20 5
rs1333049 0.715 0.286 9 22125504 intergenic variant G/C snp 0.41 5
rs2943634 0.801 0.107 2 226203364 intergenic variant A/C,G snp 0.61; 5.6E-03 5
rs4803750 0.821 0.214 19 44744370 intergenic variant A/G snp 7.3E-02 5
rs10913469 1.000 0.071 1 177944384 intron variant T/C snp 0.21 5
rs11075990
FTO
0.923 0.107 16 53785981 intron variant A/G snp 0.41 5