Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2854275 0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02 4
rs7192 0.827 0.200 6 32443869 missense variant T/G snv 0.64 0.61 7
rs7194 0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 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
rs2239802 0.882 0.200 6 32444069 intron variant C/A;G;T snv 4
rs2239803 0.882 0.240 6 32444056 intron variant C/A;T snv 0.50 4
rs3129888 0.882 0.240 6 32443949 intron variant G/A snv 0.82 0.80 4
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
rs4935356 1.000 0.080 6 32444611 intron variant T/A;G snv 2
rs7195 1.000 0.040 6 32444762 3 prime UTR variant A/G snv 0.61 2
rs8084 1.000 0.120 6 32443258 splice acceptor variant A/C;T snv 0.61; 8.1E-06 2
rs9268658 1.000 0.040 6 32442939 intron variant G/A;C snv 2
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs477515 0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs28366298 0.925 0.120 6 32593082 upstream gene variant A/C;T snv 3
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs9268832 0.882 0.160 6 32460012 non coding transcript exon variant T/C snv 0.61 0.59 4
rs9368726 6 32470765 intron variant T/C snv 0.29 1
rs9405108 6 32470871 intron variant C/T snv 0.29 1
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1161098 12 67453680 intron variant G/A snv 0.84 1
rs9267536 6 31683417 intron variant A/C snv 5.3E-02 1