Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 7
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 6
rs62081501 0.925 0.080 18 37627749 intron variant G/A snv 6.2E-02 4
rs10801153 0.925 0.080 1 192794818 intron variant G/A snv 0.27 3
rs2572431 1.000 0.040 8 11247568 downstream gene variant C/G;T snv 2
rs34548976 1.000 0.040 7 31032854 intergenic variant C/T snv 0.39 2
rs4684833 1.000 0.040 3 11990245 intergenic variant C/T snv 0.79 2
rs4813627 1.000 0.040 20 3074867 downstream gene variant A/G snv 0.51 2
rs483143 0.925 0.080 6 27878966 intergenic variant G/C snv 0.13 2
rs80533 1.000 0.040 22 40689965 intergenic variant A/G snv 0.81 2
rs11159097 1.000 0.040 14 74633180 intergenic variant T/A;C snv 1
rs11204421 1.000 0.040 17 19994492 intergenic variant T/C snv 0.44 1
rs11663050 1.000 0.040 18 37621190 intron variant T/G snv 0.51 1
rs12145083 1.000 0.040 1 197853864 intergenic variant T/A snv 0.17 1
rs12484971 1.000 0.040 22 41043300 upstream gene variant A/T snv 0.25 1
rs1330745 1.000 0.040 13 58585815 intergenic variant A/C snv 0.15 1
rs13324323 1.000 0.040 3 166989488 intergenic variant C/T snv 0.23 1
rs1427041 1.000 0.040 18 37628357 intron variant A/G;T snv 1
rs150491901 1.000 0.040 8 10468395 intergenic variant G/A;T snv 1
rs16902946 1.000 0.040 5 87982999 intron variant T/C snv 0.22 1
rs1826787 1.000 0.040 10 105908635 downstream gene variant C/T snv 0.16 1
rs2407746 1.000 0.040 8 5080235 regulatory region variant C/G snv 0.28 1
rs246914 1.000 0.040 5 103223706 intergenic variant T/C snv 0.17 1
rs2672852 1.000 0.040 2 103455652 intergenic variant C/T snv 0.44 1
rs3124377 1.000 0.040 13 55411477 intergenic variant C/T snv 0.63 1