Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs13361189 0.752 0.240 5 150843825 upstream gene variant T/C snv 0.21 13
rs1495741 0.827 0.240 8 18415371 regulatory region variant G/A snv 0.71 9
rs2737190 0.827 0.120 9 117701903 upstream gene variant G/A snv 0.52 6
rs4842407 0.882 0.200 12 78807293 intron variant A/G snv 0.35 4
rs7194886 0.851 0.080 16 50691282 upstream gene variant C/T snv 0.38 4
rs11031731 0.925 0.040 11 32343884 upstream gene variant G/A snv 0.18 3
rs160441 1.000 0.040 8 89644760 intron variant T/C snv 0.55 2
rs218916 1.000 0.040 8 89688709 intron variant C/T snv 0.67 2
rs35037722 0.925 0.040 17 78355453 upstream gene variant G/A;C snv 2
rs4331426 0.925 0.080 18 22610832 intergenic variant G/A snv 0.86 2
rs6610650 1.000 0.040 X 37777261 intron variant G/A snv 0.27 2
rs8073782 0.925 0.040 17 27807685 intron variant C/T snv 0.27 2
rs1075309 1.000 0.040 2 5113465 intergenic variant C/T snv 0.20 1
rs11031728 1.000 0.040 11 32342070 intron variant C/G snv 0.18 1
rs12437118 1.000 0.040 14 76517387 intron variant G/A;C snv 1
rs12456774 1.000 0.040 18 22592612 intergenic variant G/A snv 0.17 1
rs17175227 1.000 0.040 14 70035333 downstream gene variant G/A;C snv 2.1E-02 1
rs2057178 1.000 0.040 11 32342641 intron variant G/A snv 0.18 1
rs2202157 1.000 0.040 3 26501929 intergenic variant C/T snv 0.12 1
rs39509 1.000 0.040 8 89791937 downstream gene variant G/A snv 0.65 1
rs4859843 1.000 0.040 4 77439033 intron variant T/C;G snv 1
rs4859846 1.000 0.040 4 77439174 intron variant G/A snv 0.19 1
rs6676375 1.000 0.040 1 242711583 intergenic variant T/C snv 0.15 1
rs8087945 1.000 0.040 18 22596123 intergenic variant A/G snv 0.61 1