Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
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
rs1059513 0.776 0.240 12 57095926 3 prime UTR variant T/C snv 8.0E-02 6
rs7936323 0.882 0.160 11 76582714 intergenic variant G/A snv 0.44 6
rs3785356 0.925 0.080 16 27337847 intron variant C/T snv 0.25 5
rs55646091 0.925 0.080 11 76588387 upstream gene variant G/A snv 3.0E-02 5
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
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 3
rs2381416 1.000 0.080 9 6193455 upstream gene variant C/A snv 0.65 3
rs61840192 1.000 0.080 10 9001441 intergenic variant G/A;C;T snv 3