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
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
rs3791679 0.925 0.120 2 55869757 intron variant A/G snv 0.20 8
rs2710323 0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs7531118 1.000 0.080 1 72371556 intron variant T/C snv 0.40 7
rs10195252 0.925 0.080 2 164656581 intron variant T/C snv 0.48 6
rs55872725
FTO
16 53775211 intron variant C/T snv 0.31 6
rs7133378 12 123924955 intron variant G/A snv 0.38 6
rs1812175 4 144653692 intron variant A/G snv 0.79 5
rs2371767 3 64732582 intron variant G/C snv 0.38 5
rs3786897 1.000 0.080 19 33402102 intron variant A/G snv 0.45 5
rs395962 6 104949543 intron variant T/G snv 0.72 5
rs4130548 1.000 0.040 1 77998184 intron variant T/C snv 0.25 5
rs633715 1.000 0.080 1 177883445 intron variant T/C snv 0.17 5
rs7141420 1.000 0.080 14 79433111 intron variant C/T snv 0.56 5
rs7801581 7 27184152 intron variant C/T snv 0.24 5
rs987237 0.925 0.120 6 50835337 intron variant A/G snv 0.17 5
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 5
rs10842707 12 26318431 intron variant C/G;T snv 4
rs10923712 1 118962811 intron variant G/A snv 0.56 4
rs12429545 13 53528071 intron variant G/A;T snv 0.12 4
rs17024393 1 109612066 intron variant T/C snv 4.6E-02 4
rs1936807 6 127127104 intron variant C/G snv 0.55 4
rs2033529 6 40380914 intron variant A/C;G snv 4