Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 21
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs2241423 0.882 0.120 15 67794500 intron variant G/A snv 0.29 7
rs2030323 0.925 0.080 11 27706992 intron variant A/C snv 0.83 6
rs2535633 1.000 0.080 3 52825614 intron variant C/G snv 0.48 4