Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs3771180 1.000 0.080 2 102337157 5 prime UTR variant G/A;T snv 2
rs10173081 1.000 0.080 2 102340888 intron variant C/T snv 0.18 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
rs13431828 0.925 0.160 2 102338193 5 prime UTR variant C/T snv 0.18 2
rs1420101 0.827 0.280 2 102341256 synonymous variant C/T snv 0.33 0.35 2
rs3771175 0.925 0.080 2 102343750 3 prime UTR variant T/A snv 0.18 2
rs10204137 0.925 0.160 2 102351752 missense variant A/G;T snv 0.34 1
rs10208293 0.882 0.160 2 102349850 intron variant G/A snv 0.33 1
rs12479210 1.000 0.080 2 102332701 intron variant C/A;T snv 1