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 5
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 6
rs10800314 0.827 0.120 1 161502999 upstream gene variant C/A snv 0.65 5
rs10995271 0.776 0.280 10 62678726 downstream gene variant G/C snv 0.32 5
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
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 5
rs11749040 0.827 0.120 5 40396323 regulatory region variant G/A snv 0.15 5
rs12188300 0.807 0.120 5 159402519 intron variant A/G;T snv 6
rs12879003 0.827 0.120 14 35359535 downstream gene variant T/A;G snv 0.43 5
rs12932970 0.827 0.120 16 85970504 intron variant T/C snv 0.29 5
rs1405108 0.827 0.120 2 198880294 downstream gene variant C/A snv 0.61 5
rs1569328 0.827 0.120 14 75275048 upstream gene variant C/T snv 0.12 6
rs16967103 0.827 0.120 15 38606989 intergenic variant T/C snv 0.22 6
rs17085007 0.827 0.120 13 26957130 regulatory region variant T/C snv 0.16 6
rs1992661 0.827 0.120 5 40414887 upstream gene variant G/A snv 0.58 5
rs2042011 0.827 0.120 8 128215706 upstream gene variant A/G snv 0.39 5