Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 2
rs17498196 1.000 0.080 9 6237547 intron variant A/C;G snv 2
rs10197862 0.925 0.120 2 102350089 intron variant A/G snv 0.18 2
rs204993 0.851 0.240 6 32187804 intron variant A/G snv 0.24 0.26 3
rs3806932 0.925 0.160 5 111069977 upstream gene variant A/G snv 0.51 2
rs3816470 0.925 0.160 17 39829548 intron variant A/G snv 0.54 3
rs7130588 0.882 0.200 11 76559639 regulatory region variant A/G snv 0.29 3
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs9909593 0.925 0.160 17 39813896 intron variant A/G snv 0.38 3
rs4794820 0.790 0.160 17 39933091 intron variant A/G;T snv 3
rs992969 0.882 0.080 9 6209697 intergenic variant A/G;T snv 2
rs10189629 1.000 0.080 2 102263004 regulatory region variant C/A snv 0.15 2
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 2
rs1464510
LPP
0.807 0.280 3 188394766 intron variant C/A;T snv 7
rs1362348 1.000 0.080 2 102368164 intron variant C/G snv 0.45 2
rs12936231 0.925 0.160 17 39872867 intron variant C/G;T snv 3
rs10173081 1.000 0.080 2 102340888 intron variant C/T snv 0.18 2
rs10192157 1.000 0.080 2 102351896 missense variant C/T snv 0.34 0.46 2
rs10445308 0.851 0.240 17 39781794 intron variant C/T snv 0.38 3
rs11078927 0.925 0.080 17 39908152 intron variant C/T snv 0.40 0.35 2
rs11557466 0.925 0.160 17 39868373 synonymous variant C/T snv 0.40 0.36 3
rs11692065 1.000 0.080 2 102267515 intergenic variant C/T snv 0.15 2
rs13431828 0.925 0.160 2 102338193 5 prime UTR variant C/T snv 0.18 2
rs2305479 0.882 0.160 17 39905964 missense variant C/T snv 0.43 0.39 4
rs3755276 0.925 0.120 2 102361999 intron variant C/T snv 0.45 2