Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1059513 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 11
rs112401631 0.882 0.120 17 40608272 TF binding site variant T/A snv 1.1E-02 8
rs34290285 0.851 0.120 2 241759225 intron variant G/A snv 0.27 8
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs4821544 0.925 0.040 22 36862461 intron variant T/A;C snv 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs2033784 1.000 0.080 15 67157322 intron variant A/G snv 0.35 4
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 4
rs1057258 2 233206983 3 prime UTR variant C/T snv 0.30 3
rs346835 2 8298563 intron variant C/T snv 0.39 3
rs6021268 20 51524602 intron variant T/C snv 5.8E-02 3