Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72823641 0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs7928663 1.000 0.080 11 102321236 intron variant C/T snv 0.72 1
rs12479210 1.000 0.080 2 102332701 intron variant C/A;T snv 2
rs7127583 1.000 0.080 11 102334306 intron variant T/C snv 0.71 1
rs3771180 1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv 2
rs3460 1.000 0.080 11 102337659 3 prime UTR variant G/C snv 8.3E-02 1
rs13431828 0.925 0.160 2 102338193 5 prime UTR variant C/T snv 0.18 3
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
rs1041973 1.000 0.080 2 102339008 missense variant C/A snv 0.23 0.30 1
rs10173081 1.000 0.080 2 102340888 intron variant C/T snv 0.18 2
rs1420101 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 8
rs3771175 0.925 0.080 2 102343750 3 prime UTR variant T/A snv 0.18 3
rs201256810 0.925 0.080 2 102348073 missense variant C/T snv 2
rs10208293 0.882 0.160 2 102349850 intron variant G/A snv 0.33 4
rs10197862 0.925 0.120 2 102350089 intron variant A/G snv 0.18 3
rs1861245 0.925 0.080 2 102350446 intron variant C/T snv 2
rs10204137 0.925 0.160 2 102351752 missense variant A/G;T snv 0.34 2
rs10192157 1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 2
rs10206753 1.000 0.080 2 102351902 missense variant T/C;G snv 0.34; 4.0E-06 2
rs9807989 1.000 0.080 2 102354740 intron variant T/C;G snv 0.46 2
rs3755276 0.925 0.120 2 102361999 intron variant C/T snv 0.45 3
rs1362348 1.000 0.080 2 102368164 intron variant C/G snv 0.45 2
rs3771166 1.000 0.080 2 102369762 intron variant G/A;T snv 2
rs2241116 1.000 0.080 2 102386805 intron variant C/A;T snv 1