Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1432441 0.882 0.040 15 66426943 intron variant G/A snv 0.27 3
rs1549854 0.882 0.040 15 66404397 intron variant A/C;G snv 0.44 3
rs1488864 0.851 0.080 11 6321099 intron variant T/G snv 0.80 4
rs11904814 0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs174697 0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs61888800 0.851 0.080 11 27700731 5 prime UTR variant G/T snv 0.19 5
rs794727961 0.851 0.080 12 2512979 missense variant G/A snv 5
rs9825823 0.851 0.080 3 61096480 intron variant T/C snv 0.47 5
rs10514299 0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs1545843 0.827 0.120 12 84170289 intron variant G/A snv 0.52 6
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs120074175 0.827 0.080 12 72031544 missense variant G/A snv 1.2E-05 7.0E-06 7
rs2522833 0.827 0.080 7 82824392 missense variant A/C snv 0.45 0.34 7
rs7305115 0.807 0.200 12 71979082 synonymous variant A/C;G;T snv 4.0E-06; 0.56 8
rs2242446 0.776 0.080 16 55656513 5 prime UTR variant C/A;T snv 9
rs9722 0.776 0.200 21 46599326 3 prime UTR variant G/A snv 0.16; 2.4E-05 0.21 9
rs11030101 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs4713916 0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs7997012 0.807 0.080 13 46837850 intron variant A/G snv 0.69 11
rs1800532 0.763 0.160 11 18026269 intron variant G/T snv 0.33 15
rs2230912 0.752 0.280 12 121184393 missense variant A/G snv 0.13 0.12 16
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs1805054 0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
rs1176744 0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19