Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 12
rs543874 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 11
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 11
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 9
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs2820443 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 8
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs112875651 8 125494452 intron variant G/A snv 0.31 7
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs10132280 14 25458973 intergenic variant C/A snv 0.37 6
rs605066 6 139508529 intron variant C/T snv 0.53 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs7166081 0.925 0.080 15 67199963 downstream gene variant G/A snv 0.76 6
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 6
rs10804591 3 129615390 intergenic variant C/A snv 0.63 5
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 5
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs634869 6 139510620 intron variant T/A;C snv 5
rs6556301 5 177100576 downstream gene variant G/T snv 0.33 5
rs7536458 1 118321979 intergenic variant T/G snv 0.23 5
rs10245353 7 25818994 intergenic variant C/A snv 0.16 4