Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12232497 0.701 0.360 17 39883866 intergenic variant T/C snv 0.35 18
rs7725052 0.716 0.240 5 40487168 intron variant C/T snv 0.52 16
rs2155219 0.732 0.280 11 76588150 upstream gene variant G/T snv 0.52 14
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs2872507 0.752 0.360 17 39884510 intergenic variant G/A;T snv 12
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs7927894 0.742 0.320 11 76590272 upstream gene variant C/T snv 0.35 12
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 10
rs1342326 0.790 0.360 9 6190076 intergenic variant A/C snv 0.21 9
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 7
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs13437088 0.925 0.040 6 31387342 intergenic variant C/T snv 0.32 6
rs17454584 0.851 0.080 4 122432277 downstream gene variant A/G snv 0.17 6
rs479844 0.851 0.160 11 65784486 upstream gene variant A/G snv 0.44 6
rs7775759 0.925 0.200 6 31384669 upstream gene variant G/A snv 0.36 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs9687958 0.827 0.120 5 40496321 intron variant G/T snv 0.60 6
rs10947207 1.000 6 31393708 downstream gene variant T/C snv 0.31 5
rs12365699 0.882 0.120 11 118872577 regulatory region variant G/A snv 0.12 5
rs4711268 1.000 6 31386727 upstream gene variant C/T snv 0.31 5