Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs10514299 0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs110402 0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs1137070 0.763 0.160 X 43744144 synonymous variant T/C snv 0.62 9
rs115357105 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 4
rs11568817 0.790 0.120 6 77463665 5 prime UTR variant A/C snv 0.37 8
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs11825659 0.925 0.080 11 133925624 intron variant A/G snv 0.12 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12180309 0.925 0.080 6 91209048 intergenic variant C/T snv 1.9E-02 4
rs12544026 0.925 0.080 8 101819970 intron variant G/A snv 0.85 4
rs12898460 0.882 0.080 15 38694612 intron variant C/T snv 0.23 3
rs12912251 0.882 0.080 15 38694167 intron variant G/T snv 0.25 3
rs130058 0.790 0.120 6 77463564 5 prime UTR variant T/A;G snv 8
rs139438618 0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 5
rs1535255 0.807 0.120 6 88151489 intron variant T/G snv 0.21 8
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs173365 0.882 0.080 17 45823708 intron variant A/G snv 0.55 3
rs1800532 0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs1824024 0.851 0.160 7 136958947 intron variant C/A snv 0.65 4
rs2061174 0.882 0.080 7 136976653 intron variant G/A;C snv 3
rs2094081 0.925 0.080 1 38927359 intron variant G/A;C snv 4
rs2273816 0.851 0.080 13 49719920 intron variant G/A;C snv 4
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs3219151 0.752 0.160 5 161701908 3 prime UTR variant C/T snv 0.51 14