Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4785763 0.925 0.120 16 90000528 non coding transcript exon variant A/C;T snv 3
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs3803662 0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs2981582 0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs13387042 0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs10993994 0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 15
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs132770 0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs4430796 0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs7014346 0.732 0.240 8 127412547 intron variant A/G snv 0.63 14
rs3021097 0.752 0.440 1 206773289 5 prime UTR variant A/G snv 10
rs8042374 0.807 0.200 15 78615690 intron variant A/G snv 0.29 10
rs11978267 0.763 0.240 7 50398606 intron variant A/G snv 0.25 9
rs7023329 0.790 0.160 9 21816529 intron variant A/G snv 0.50 9
rs80358259 0.851 0.320 18 23536736 missense variant A/G snv 2.0E-04 2.4E-04 9
rs995030 0.776 0.320 12 88496894 3 prime UTR variant A/G snv 0.67 9
rs2981579 0.776 0.280 10 121577821 intron variant A/G snv 0.53 8
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 7