Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6784615 1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 1
rs1034207 6 127016554 intron variant C/A;G;T snv 0.94 1
rs1993709 1.000 0.080 1 72372846 intron variant A/G snv 0.85 1
rs4686340 3 9303534 intron variant A/C snv 0.80 1
rs605203 1.000 0.120 6 31879235 intron variant C/A snv 0.77 1
rs645040 3 136207780 upstream gene variant G/T snv 0.77 1
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 1
rs7647305 1.000 0.080 3 186116501 intron variant T/C snv 0.74 3
rs1020731 1.000 0.080 2 160287544 intron variant G/A snv 0.69 1
rs459193 0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1
rs9931989 16 28894763 intron variant G/C snv 0.68 3
rs9369425 0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 3
rs1294410 6 6738519 intron variant T/C snv 0.65 1
rs9515201 0.925 0.080 13 110388451 intron variant A/C snv 0.63 1
rs11102800 1.000 0.040 1 114498310 intron variant C/T snv 0.58 1
rs7745274 6 127188012 intron variant G/A snv 0.56 1
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs6486060 11 9003083 intron variant G/A snv 0.55 1
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 3
rs605066 6 139508529 intron variant C/T snv 0.53 4
rs10195252 0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs13389219 1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs1011731 1 172377408 intron variant G/A snv 0.46 1
rs9491696 6 127131494 intron variant C/G snv 0.45 1
rs3786897 1.000 0.080 19 33402102 intron variant A/G snv 0.45 1