Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs6457617 0.763 0.480 6 32696074 intergenic variant C/A;T snv 11
rs398652 0.752 0.240 14 56058851 intergenic variant G/A snv 0.24 10
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 8
rs3135363 0.776 0.360 6 32421871 intergenic variant A/G snv 0.24 8
rs2647012 0.790 0.320 6 32696681 intergenic variant T/C snv 0.64 7
rs10484561 0.827 0.160 6 32697643 intergenic variant T/G snv 0.13 6
rs7774434 0.807 0.360 6 32689801 TF binding site variant T/C snv 0.40 6
rs9275312 0.807 0.280 6 32697951 intergenic variant A/G snv 0.16 6
rs9275319 0.807 0.200 6 32698518 intergenic variant A/G snv 0.15 6
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs2856683 0.827 0.320 6 32687441 regulatory region variant T/A;C;G snv 0.25 5
rs10116253 0.851 0.120 9 117702042 upstream gene variant T/C snv 0.28 4
rs2069852 0.925 0.080 7 22732641 downstream gene variant G/A;C snv 4
rs5000634 0.851 0.200 6 32695787 intergenic variant A/G snv 0.39 4
rs17007417 0.882 0.080 2 71808541 regulatory region variant T/C snv 0.85 3
rs2148356 1.000 0.080 9 7395038 intergenic variant G/A;C snv 2
rs2856723 0.925 0.120 6 32699985 intergenic variant A/G snv 0.63 2
rs3094137 0.925 0.120 6 30233096 downstream gene variant A/G;T snv 2
rs4309483 0.925 0.120 18 58418685 downstream gene variant A/C snv 0.70 2
rs4985790 0.925 0.120 17 21420842 downstream gene variant G/A snv 2
rs7708357 1.000 0.080 5 177104771 intergenic variant A/G snv 0.58 2
rs9271568 0.925 0.200 6 32622686 TF binding site variant G/A snv 0.27 2