Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs184003 0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2070895 0.807 0.120 15 58431740 intron variant G/A snv 0.33 15
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs2072668 0.732 0.280 3 9756456 intron variant C/G snv 0.28 0.24 14
rs2149356 0.742 0.360 9 117711921 intron variant T/G snv 0.54 14
rs2201841 0.716 0.440 1 67228519 intron variant A/G;T snv 14
rs4430796 0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs6887695 0.732 0.440 5 159395637 intron variant G/C snv 0.35 14
rs4580704 0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs4704397 0.807 0.200 5 77222617 intron variant G/A snv 0.54 13
rs6742078 0.807 0.240 2 233763993 intron variant G/T snv 0.36 13
rs7044343 0.752 0.520 9 6254208 intron variant C/T snv 0.51 13
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs10423928 0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs7501939 0.776 0.280 17 37741165 intron variant C/T snv 0.41 12
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs864745 0.763 0.320 7 28140937 intron variant T/C snv 0.41 12
rs972936 0.807 0.200 12 102431143 intron variant T/C snv 0.70 12
rs10911021 0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs5742612 0.752 0.440 12 102481086 intron variant A/G snv 5.6E-02 11
rs6908425 0.752 0.320 6 20728500 intron variant T/C snv 0.78 11
rs10968576 0.882 0.120 9 28414341 intron variant A/G snv 0.26 10
rs1128249 1.000 0.080 2 164672114 intron variant G/C;T snv 10
rs13333226 0.827 0.200 16 20354332 intron variant A/G snv 0.23 10