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 61
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs34536443 0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs4676410 0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs4246905 0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs4246215 0.677 0.320 11 61796827 3 prime UTR variant G/C;T snv 13
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 11
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 10
rs7495132 0.790 0.080 15 90629669 intron variant C/T snv 0.12 10
rs516246 0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs4845604 0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs11221332 0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs11168249 0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs17622378 0.790 0.200 5 132442760 intron variant A/G snv 0.28 8