Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs17446593 1.000 0.080 13 40553948 intron variant A/G snv 0.19 2
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs11061946 1.000 0.080 12 1719361 intron variant C/T snv 6.8E-02 2
rs11061973 1.000 0.080 12 1756770 intron variant G/A snv 0.12 2
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs2278426 1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs945508 1.000 0.080 1 156937289 missense variant T/C snv 0.64 0.66 3
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs3731201 1.000 0.080 9 21988897 intron variant C/T snv 0.86 2
rs495490 1.000 0.080 9 22010413 intron variant A/G snv 6.8E-02 2
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs997509 0.827 0.200 6 131846837 intron variant C/T snv 5.3E-02 6
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs17446614 0.851 0.240 13 40565740 intron variant G/A snv 0.16 5
rs2297627 0.925 0.120 13 40659794 intron variant A/G snv 0.41 3
rs2721068 0.882 0.160 13 40565575 intron variant T/C snv 0.38 4
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1801483 0.851 0.160 17 81809839 missense variant G/A snv 7.4E-03 6.3E-03 7
rs773641005 0.742 0.240 16 58723829 missense variant T/C snv 14
rs1169288 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs3813929 0.851 0.240 X 114584047 upstream gene variant C/G;T snv 5