Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178 0.692 0.429 12 111569952 intron variant C/T snp 0.67 16
rs2476601 0.547 0.750 1 113834946 missense variant A/G snp 0.93 0.92 10
rs9939609
FTO
0.580 0.607 16 53786615 intron variant T/A snp 0.42 10
rs2187668 0.724 0.393 6 32638107 intron variant C/T snp 10
rs9268853 0.801 0.250 6 32461866 intron variant T/C snp 0.27 9
rs2395185 0.756 0.321 6 32465390 intron variant G/T snp 0.27 8
rs2542151 0.734 0.286 18 12779948 intergenic variant G/T snp 0.83 8
rs2872507 0.769 0.214 17 39884510 intergenic variant G/A,T snp 0.39 7
rs1893217 0.801 0.214 18 12809341 intron variant A/G snp 0.13 7
rs2305480 0.821 0.214 17 39905943 missense variant G/A snp 0.40 0.35 6
rs1464510
LPP
0.821 0.250 3 188394766 intron variant C/A,T snp 0.41; 1.0E-02 6
rs3197999 0.724 0.250 3 49684099 missense variant G/A snp 0.26 0.26 6
rs13003464 0.821 0.179 2 60959694 intron variant A/G snp 0.48 6
rs10758669 0.784 0.214 9 4981602 intergenic variant C/A,T snp 0.70 5
rs10938397 0.846 0.179 4 45180510 intergenic variant A/G snp 0.38 5
rs2155219 0.756 0.250 11 76588150 regulatory region variant G/T snp 0.52 5
rs2327832 0.801 0.286 6 137651931 intergenic variant A/G snp 0.16 5
rs3129890 0.846 0.179 6 32446496 intergenic variant T/A,C snp 0.30 5
rs7775228 0.801 0.321 6 32690302 intergenic variant T/C snp 0.15 5
rs7927894 0.821 0.214 11 76590272 intergenic variant C/T snp 0.34 5
rs8067378 0.769 0.179 17 39895095 intergenic variant A/G snp 0.50 5
rs917997 0.734 0.321 2 102454108 intergenic variant T/A,C snp 0.79 5
rs1801274 0.679 0.429 1 161509955 missense variant A/C,G snp 4.0E-06; 0.48 0.51 5
rs2290400 0.821 0.286 17 39909987 intron variant T/C snp 0.48 5
rs9272346 0.821 0.286 6 32636595 intron variant G/A snp 5