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
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
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
rs3115663 0.827 0.360 6 31634066 non coding transcript exon variant T/C snv 0.17 7
rs7194 0.827 0.280 6 32444703 3 prime UTR variant G/A snv 0.61 7
rs2395182 0.851 0.280 6 32445540 downstream gene variant G/T snv 0.76 5
rs10947261 0.882 0.240 6 32405455 splice region variant G/T snv 0.11 4
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 4
rs2239803 0.882 0.240 6 32444056 intron variant C/A;T snv 0.50 4
rs2854275 0.925 0.120 6 32660651 non coding transcript exon variant C/A snv 9.6E-02 4
rs10947262 0.925 0.040 6 32405535 non coding transcript exon variant C/T snv 0.12 3
rs12759054 1.000 0.040 1 233984064 intron variant T/A;C snv 3
rs2294881 1.000 0.040 6 32399827 intron variant T/C snv 0.19 3
rs28366298 0.925 0.120 6 32593082 upstream gene variant A/C;T snv 3
rs3130048 1.000 0.120 6 31645962 intron variant T/C snv 0.23 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
rs2294882 6 32399738 intron variant T/C snv 0.19 2
rs4248166 1.000 0.040 6 32398644 intron variant T/C snv 0.18 2
rs4935356 1.000 0.080 6 32444611 intron variant T/A;G snv 2
rs6901541 1.000 0.120 6 32474484 upstream gene variant T/C;G snv 2