Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 17
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2516049 0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 12
rs652888 0.776 0.480 6 31883457 non coding transcript exon variant A/G snv 0.18 0.20 10
rs477515 0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 10
rs9268853 0.790 0.440 6 32461866 intron variant T/C snv 0.29 10
rs3130618 0.827 0.360 6 31664357 missense variant C/A;T snv 0.15; 4.0E-06 7
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
rs3115663 0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 7
rs11229 0.851 0.280 6 31635993 synonymous variant A/G snv 0.14 0.17 6
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
rs2227139 0.925 0.160 6 32445682 downstream gene variant G/A snv 0.61 4
rs10947261 0.882 0.240 6 32405455 splice region variant G/T snv 0.11 4
rs1048369 0.882 0.160 X 133303309 missense variant G/A snv 0.33 0.38 4
rs2854275 0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02 4
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
rs9268832 0.882 0.160 6 32460012 non coding transcript exon variant T/C snv 0.61 0.59 4
rs204994 0.925 0.120 6 32187221 non coding transcript exon variant C/T snv 0.18 0.21 4
rs3117583 0.925 0.200 6 31651799 5 prime UTR variant A/G snv 0.14 0.17 3