Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800728 0.807 0.080 1 94011395 intron variant A/G snv 2.3E-04 3.0E-04 8
rs560426 0.851 0.200 1 94087882 intron variant C/T snv 0.53 5
rs11806129 1 94016821 intron variant A/G;T snv 3
rs12087003 1 94037627 intron variant A/G snv 6.3E-02 3
rs481931 0.882 0.120 1 94104460 intron variant G/T snv 0.32 3
rs66515264 0.882 0.120 1 94092554 intron variant G/A;T snv 3
rs778234759 0.925 0.040 1 94018445 intron variant C/T snv 1.3E-04 3
rs17110922 1 94043489 intron variant A/T snv 2.5E-03 9.9E-03 2
rs3789432 0.925 0.080 1 94109752 intron variant T/C snv 0.33 2
rs137866734 1 94074274 intron variant C/T snv 6.8E-03 1
rs1457937638 1.000 1 94027444 intron variant C/A;T snv 1
rs3789451 1.000 0.080 1 94120772 intron variant C/G;T snv 1
rs3827712 1.000 0.080 1 94109615 intron variant T/C;G snv 1
rs4147811 1.000 0.080 1 94109500 intron variant C/T snv 0.33 1
rs4147812 1.000 0.080 1 94109487 intron variant A/C;T snv 1
rs4147816 1.000 0.080 1 94109224 intron variant C/T snv 0.33 1
rs570926 1.000 0.080 1 94104662 intron variant T/C snv 0.39 1
rs952499 1.000 0.080 1 94092869 intron variant T/C snv 0.45 1
rs61751383 0.827 0.080 1 94005500 stop gained G/A snv 2.8E-05 1.4E-05 6
rs61750654 0.925 0.120 1 94000870 stop gained G/A snv 2.0E-05 7.0E-06 5
rs61753038 0.851 0.080 1 94005470 stop gained G/A snv 1.2E-05 7.0E-06 4
rs61749414 0.882 0.080 1 94062611 stop gained G/A;T snv 3
rs61749423 0.925 0.040 1 94060656 stop gained G/A;T snv 8.0E-06; 4.4E-05 3
rs61749455 0.882 0.080 1 94044692 stop gained C/A;G;T snv 5.6E-04; 4.0E-06 3
rs1553192726 1.000 0.080 1 94063315 stop gained G/T snv 2