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 22
rs137852578
AR
0.827 0.080 X 67723710 missense variant A/G snv 2
rs1057519912 0.776 0.200 X 71129408 missense variant C/G;T snv 5
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 8
rs137852581
AR
0.882 0.080 X 67723701 missense variant C/T snv 2
rs486907 0.667 0.360 1 182585422 missense variant C/T snv 0.31 0.28 1
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs121913430 1.000 0.080 7 55174740 missense variant G/A snv 2
rs17366568 0.851 0.200 3 186852664 non coding transcript exon variant G/A snv 8.8E-02 1
rs182052 0.701 0.440 3 186842993 intron variant G/A snv 0.38 1
rs786202601 1.000 0.120 22 28694059 frameshift variant T/- delins 2
rs1512268 0.851 0.160 8 23668950 intergenic variant T/C snv 0.50 3
rs28909982 0.925 0.080 22 28725338 missense variant T/C snv 1.2E-04 9.1E-05 2
rs339331 0.882 0.080 6 116888889 intron variant T/C snv 0.28 2
rs1057519971 1.000 0.080 17 49619326 missense variant T/C;G snv 1