Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 9
rs2925979 1.000 0.080 16 81501185 intron variant T/A;C snv 9
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs10195252 0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 5
rs3786897 1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs3843467 1.000 0.080 5 56560548 intron variant G/T snv 0.21 2