Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 32
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs368234815 0.742 0.280 19 39248514 frameshift variant TT/G;T delins 15
rs1057519912 0.776 0.200 X 71129408 missense variant C/G;T snv 11
rs3774261 0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 10
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs976306779
AR
0.851 0.080 X 67545492 missense variant C/A;T snv 6.6E-06 8
rs17366568 0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 6
rs1571801 0.827 0.120 9 121665094 intron variant G/T snv 0.21 6
rs1512268 0.851 0.160 8 23668950 intergenic variant T/C snv 0.50 6
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv 5
rs28909982 0.925 0.080 22 28725338 missense variant T/C snv 1.2E-04 9.1E-05 4
rs1197734477 0.925 0.080 10 87961012 missense variant A/G snv 4
rs339331 0.882 0.080 6 116888889 intron variant T/C snv 0.28 4
rs1060501201 0.925 0.080 17 7674190 missense variant T/C;G snv 4
rs786202601 1.000 0.120 22 28694059 frameshift variant T/- delins 3
rs375118292 0.925 0.080 2 224506080 missense variant T/A;C snv 2.0E-05 3
rs121913430 1.000 0.080 7 55174740 missense variant G/A snv 3
rs746001963
ERG
0.925 0.080 21 38383659 missense variant A/T snv 4.0E-06 3
rs727502792 0.925 0.080 17 49601958 missense variant T/A snv 3