Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519893 0.790 0.160 12 56085070 missense variant G/A;T snv 9
rs35463555 0.776 0.160 19 50374423 intron variant G/A snv 0.29 8
rs1157 0.790 0.080 3 105576617 3 prime UTR variant G/A snv 0.16 7
rs2978974
JRK ; PSCA
0.790 0.200 8 142670446 non coding transcript exon variant G/A snv 0.38 7
rs4595552 0.790 0.080 11 125865825 intergenic variant C/G;T snv 7
rs909629195 0.790 0.080 17 38914448 missense variant C/T snv 7
rs951540403 0.790 0.080 10 94132433 missense variant G/C snv 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs28934573 0.667 0.480 17 7674241 missense variant G/A;C;T snv 4.0E-06 28
rs1057519738 0.790 0.160 17 39725079 missense variant G/A snv 4.0E-06 10
rs1057519991 0.662 0.440 17 7675076 missense variant T/A;C;G snv 4.0E-06 26
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 24
rs775066324 0.790 0.080 17 78855710 missense variant G/A;C snv 4.0E-06; 4.0E-06 7
rs1042838
PGR
0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 12
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 26
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs779162432 0.790 0.080 2 169637315 missense variant A/G snv 4.1E-06 7
rs1444424830 0.790 0.080 7 151078923 missense variant C/T snv 4.6E-06 7.0E-06 7
rs11887534 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs778985185 0.851 0.160 7 55163734 missense variant G/A snv 8.0E-06 3.5E-05 5
rs743572 0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs746702110 0.627 0.480 3 9756778 missense variant C/T snv 1.2E-05 2.8E-05 38
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36