Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs34569203 1.000 0.040 6 27186205 intergenic variant A/C snv 0.14 1
rs34644694 1.000 0.040 1 117274369 intron variant C/A snv 0.70 1
rs3897644 1.000 0.040 18 60061837 intergenic variant C/T snv 0.48 1
rs391236 1.000 0.040 5 103342372 intergenic variant A/G snv 0.24 1
rs4937872 1.000 0.040 11 112956992 upstream gene variant A/G;T snv 1
rs502652 1.000 0.040 5 101043608 intergenic variant C/T snv 0.27 1
rs525773 1.000 0.040 3 136217611 intergenic variant G/A snv 0.51 1
rs57360718 1.000 0.040 4 118015036 intergenic variant T/C snv 0.10 1
rs61991614 1.000 0.040 14 77018366 regulatory region variant G/A snv 0.21 1
rs62081537 1.000 0.040 18 37668124 intron variant T/C snv 0.16 1