Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs477515 0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 7
rs2239804 0.851 0.240 6 32443746 intron variant T/A;C snv 0.51 5
rs2395182 0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76 5
rs7194 0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 5
rs2227139 0.925 0.160 6 32445682 downstream gene variant G/A snv 0.61 4
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
rs28366298 0.925 0.120 6 32593082 upstream gene variant A/C;T snv 3
rs3129888 0.882 0.240 6 32443949 intron variant G/A snv 0.82 0.80 3
rs2213585 1.000 0.040 6 32445373 downstream gene variant G/A snv 0.61 2
rs2213586 1.000 0.040 6 32445317 downstream gene variant A/G snv 0.61 2
rs7195 1.000 0.040 6 32444762 3 prime UTR variant A/G snv 0.61 2
rs7754768 1.000 0.040 6 32452402 regulatory region variant C/T snv 0.56 2
rs9268658 1.000 0.040 6 32442939 intron variant G/A;C snv 2