Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 10
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 9
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 8
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 8
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 8
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 7
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 7
rs2305480 0.763 0.280 17 39905943 missense variant G/A snv 0.40 0.35 7
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 7
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 7
rs2327832 0.790 0.320 6 137651931 intergenic variant A/G snv 0.16 6
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6