Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10173081 1.000 0.080 2 102340888 intron variant C/T snv 0.18 2
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 2
rs10192157 1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 2
rs10197862 0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs10206753 1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06 2
rs1043828 1.000 0.080 5 111128310 3 prime UTR variant T/C;G snv 2
rs11078927 0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 2
rs11674302 1.000 0.080 2 102270668 intergenic variant T/C snv 0.16 2
rs11692065 1.000 0.080 2 102267515 intergenic variant C/T snv 0.15 2
rs13408569 1.000 0.080 2 102338596 intron variant G/C snv 0.18 2
rs13408661 1.000 0.080 2 102338622 intron variant G/A snv 0.18 2
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs13431828 0.925 0.160 2 102338193 5 prime UTR variant C/T snv 0.18 2
rs1362348 1.000 0.080 2 102368164 intron variant C/G snv 0.45 2
rs17498196 1.000 0.080 9 6237547 intron variant A/C;G snv 2
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 2
rs1888909 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 2
rs2066362 1.000 0.080 9 6219176 intron variant G/C;T snv 2
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 2
rs3755276 0.925 0.120 2 102361999 intron variant C/T snv 0.45 2
rs3771166 1.000 0.080 2 102369762 intron variant G/A;T snv 2
rs3771180 1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv 2
rs3806932 0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51 2
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 2
rs871657 1.000 0.080 2 102154881 intron variant C/T snv 0.22 2