Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10094579 0.807 0.280 8 89837077 downstream gene variant C/A snv 0.18 6
rs10743181 0.827 0.120 11 2208529 regulatory region variant A/G snv 0.77 5
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs10750899 0.827 0.120 11 58517478 intergenic variant G/A snv 0.95 5
rs10758669 0.763 0.280 9 4981602 upstream gene variant C/A;T snv 10
rs10800314 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 5
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs10865331 0.827 0.120 2 62324337 intergenic variant A/G snv 0.57 5
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 8
rs11117431 0.807 0.160 16 85981710 intron variant A/G snv 0.18 6
rs111305875 0.827 0.120 6 167098098 intron variant T/G snv 3.0E-02 5
rs11190133 0.827 0.120 10 99518968 intergenic variant C/T snv 0.26 5
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs11306716 0.827 0.120 2 203843041 intergenic variant T/-;TT delins 5
rs11616188 0.827 0.120 12 6393576 upstream gene variant G/A snv 0.30 5
rs11675538 0.827 0.120 2 65459327 intron variant C/T snv 0.29 5
rs11676348 0.790 0.160 2 218145423 regulatory region variant C/G;T snv 8
rs11749040 0.827 0.120 5 40396323 regulatory region variant G/A snv 0.15 5
rs11839053 0.724 0.240 13 106410694 intergenic variant T/C snv 7.0E-02 14
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs12570088 0.851 0.160 10 58178575 intergenic variant A/G snv 4.1E-02 4
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14