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
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 16
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs1111875 0.776 0.360 10 92703125 intergenic variant C/T snv 0.36 10
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs2081687 0.882 0.240 8 58476006 intergenic variant T/C snv 0.70 6
rs7136716 0.851 0.080 12 7538538 regulatory region variant A/G snv 0.22 6
rs10920501 0.827 0.120 1 190092815 downstream gene variant A/T snv 0.18 5
rs17128183 0.882 0.120 14 55112795 intergenic variant A/G snv 0.57 5
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 4
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 4
rs9982601 0.851 0.080 21 34226827 intron variant C/T snv 0.15 4
rs10733113 0.882 0.160 1 247459055 upstream gene variant A/G snv 0.81 3
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3
rs12449782 0.925 0.200 17 63498888 intron variant G/A snv 0.41 3
rs1544935 0.925 0.160 6 39156672 intergenic variant T/G snv 0.18 3
rs17222842 0.882 0.120 13 30765980 downstream gene variant G/A snv 6.1E-02 3
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs28451064 0.925 0.080 21 34221526 intron variant G/A snv 9.2E-02 3
rs708495 0.925 0.120 14 52302622 intergenic variant T/A snv 0.57 3