Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs3807307 0.827 0.120 7 128939148 intron variant T/C snv 0.41 6
rs919462 0.807 0.120 17 45988374 intron variant C/T snv 0.15 6
rs12531711 0.827 0.200 7 128977412 intron variant A/C;G snv 5
rs16841904 0.807 0.160 1 197732862 intron variant C/T snv 0.18 5
rs1860545 0.790 0.200 12 6337611 intron variant G/A snv 0.31 5
rs35736272 0.807 0.160 17 39876427 intron variant T/C snv 0.35 5
rs9591325 0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs13238352 0.827 0.240 7 129007888 intron variant C/T snv 9.1E-02 4
rs6659932 0.827 0.240 1 67336688 intron variant A/C snv 0.81 4
rs7208487 0.925 0.080 17 39387196 intron variant T/A;G snv 4
rs911263 0.851 0.200 14 68286876 intron variant C/T snv 0.57 4
rs11724804 0.882 0.160 4 971991 intron variant G/A snv 0.43 3
rs11889341 0.732 0.480 2 191079016 intron variant C/T snv 0.21 3
rs2290400 0.790 0.360 17 39909987 intron variant T/C snv 0.48 3
rs2293370 0.882 0.160 3 119501087 intron variant G/A snv 0.18 3
rs2395148 0.882 0.200 6 32353777 intron variant G/T snv 4.6E-02 3
rs3784099 0.807 0.320 14 68283210 intron variant G/A snv 0.43 3
rs6974491 0.807 0.120 7 37334906 intron variant G/A snv 0.14 3
rs8070723 0.851 0.240 17 46003698 intron variant A/G snv 0.18 3
rs9303277 0.790 0.240 17 39820216 intron variant C/T snv 0.52 3
rs10168266 0.776 0.400 2 191071078 intron variant C/T snv 0.19 2
rs10445308 0.851 0.240 17 39781794 intron variant C/T snv 0.38 2
rs10931468 0.925 0.080 2 190673836 intron variant C/A;G;T snv 2
rs12449852 1.000 0.080 17 39475835 intron variant A/G snv 0.79 2