Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3731217 0.763 0.320 9 21984662 intron variant A/C;T snv 10
rs3731239 0.763 0.240 9 21974219 intron variant A/G snv 0.26 10
rs3731211 9 21986848 intron variant T/A snv 0.74 7
rs3731215 9 21985772 intron variant A/G snv 1.2E-03 5
rs3731246 0.882 0.120 9 21971990 intron variant C/G snv 0.11 3
rs2518720 0.925 0.080 9 21978980 intron variant C/T snv 0.43 2
rs3731199 9 21989331 intron variant T/C snv 2.4E-03 2
rs3731201 1.000 0.080 9 21988897 intron variant C/T snv 0.86 2
rs3731236 9 21976977 intron variant G/A snv 1.9E-03 2
rs3731245 0.925 0.120 9 21972446 intron variant C/T snv 6.6E-03 2
rs1060501266 1.000 0.120 9 21968347 intron variant T/C snv 7.0E-06 1
rs2811709 1.000 0.120 9 21980152 intron variant A/G snv 0.88 1
rs2811710 1.000 0.160 9 21991924 intron variant C/T snv 0.47 1
rs4074785 1.000 0.080 9 21981584 intron variant G/A snv 0.12 1
rs61271866 1.000 0.080 9 21997016 intron variant T/A snv 0.19 1
rs7036656 9 21990458 intron variant C/T snv 0.74 1
rs34968276 0.776 0.240 9 21971110 stop gained G/A;C;T snv 9
rs121913387 0.827 0.160 9 21971187 stop gained G/A;C snv 4.6E-06 6
rs45476696 0.925 0.200 9 21970902 stop gained C/A;T snv 3
rs121913384 1.000 0.120 9 21971097 stop gained C/A;G snv 2
rs121913388 0.925 0.040 9 21971121 stop gained G/A;C snv 4.4E-06 2
rs141798398 1.000 0.120 9 21974793 stop gained G/A;T snv 2
rs730881673 1.000 0.120 9 21974696 stop gained -/T;TT delins 4.0E-06 2
rs864622636 1.000 0.120 9 21974680 stop gained G/A;T snv 2
rs876658556 1.000 0.120 9 21974784 stop gained C/T snv 2