Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs13389219 1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs3794991 1.000 0.080 19 19499787 intron variant C/G;T snv 7.4E-02 5
rs10195252 0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs2304130 1.000 0.080 19 19678719 splice region variant A/G snv 0.10 0.12 3
rs8108269 1.000 0.080 19 45655255 downstream gene variant T/G snv 0.35 2