Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3129882 0.807 0.240 6 32441753 intron variant G/A snv 0.56 5
rs3129871 0.827 0.320 6 32438565 upstream gene variant A/C snv 0.59 5
rs2395182 0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76 5
rs9268645 0.827 0.360 6 32440750 intron variant C/G;T snv 5
rs2239804 0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs7194 0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 5
rs3177928 0.882 0.120 6 32444658 3 prime UTR variant G/A snv 0.13 5
rs7192 0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61 3
rs3129888 0.882 0.240 6 32443949 intron variant G/A snv 0.82 0.80 3
rs2239802 0.882 0.200 6 32444069 intron variant C/A;G;T snv 3
rs2239803 0.882 0.240 6 32444056 intron variant C/A;T snv 0.50 3
rs6926374 0.925 0.160 6 32441528 intron variant A/G snv 0.48 2
rs3129886 0.925 0.160 6 32442799 intron variant T/A;C snv 2
rs3129883 0.925 0.160 6 32442360 intron variant T/C;G snv 0.74 2
rs3129878 0.807 0.360 6 32440958 intron variant A/C snv 0.30 2
rs3129877 0.925 0.160 6 32440820 intron variant G/A snv 0.26 2
rs3129872 0.925 0.160 6 32439376 upstream gene variant A/T snv 0.24 2
rs9268633 0.925 0.160 6 32438696 upstream gene variant A/G;T snv 2
rs9268659 0.925 0.160 6 32443164 intron variant T/C snv 0.61 0.59 2
rs3135392 0.925 0.160 6 32441465 intron variant C/A snv 0.38 2
rs8084 1.000 0.120 6 32443258 splice acceptor variant A/C;T snv 0.61; 8.1E-06 2
rs7197 0.882 0.200 6 32444803 3 prime UTR variant T/C;G snv 0.83 2
rs9268658 1.000 0.040 6 32442939 intron variant G/A;C snv 2
rs7195 1.000 0.040 6 32444762 3 prime UTR variant A/G snv 0.61 2
rs2213586 1.000 0.040 6 32445317 downstream gene variant A/G snv 0.61 2