Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1008723 0.925 0.160 17 39910014 intron variant G/C;T snv 3
rs10173081 1.000 0.080 2 102340888 intron variant C/T snv 0.18 2
rs10197862 0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs10445308 0.851 0.240 17 39781794 intron variant C/T snv 0.38 3
rs11078925 0.925 0.160 17 39868955 intron variant T/C snv 0.36 3
rs11078927 0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 2
rs11870965 0.925 0.160 17 39873952 intron variant T/A snv 0.40 3
rs12936231 0.925 0.160 17 39872867 intron variant C/G;T snv 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
rs1362348 1.000 0.080 2 102368164 intron variant C/G snv 0.45 2
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs17498196 1.000 0.080 9 6237547 intron variant A/C;G snv 2
rs204993 0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 3
rs2066362 1.000 0.080 9 6219176 intron variant G/C;T snv 2
rs2290400 0.790 0.360 17 39909987 intron variant T/C snv 0.48 6
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
rs3816470 0.925 0.160 17 39829548 intron variant A/G snv 0.54 3
rs4794820 0.790 0.160 17 39933091 intron variant A/G;T snv 3
rs4795400 0.925 0.080 17 39910767 intron variant C/T snv 0.36 3
rs4795405 0.851 0.160 17 39932164 intron variant T/A;C snv 3
rs7216389 0.732 0.440 17 39913696 intron variant C/T snv 0.60 3
rs8076131 0.790 0.200 17 39924659 intron variant G/A;C snv 3
rs869402 0.925 0.160 17 39911790 intron variant T/A;C snv 3