Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs207016 1.000 0.040 21 17270927 intergenic variant G/A snv 1.00 1
rs3759914 1.000 0.040 15 92393214 upstream gene variant C/T snv 0.97 1
rs3759916 1.000 0.040 15 92392939 upstream gene variant C/T snv 0.97 1
rs3864075 1.000 0.040 3 7659884 intron variant G/A snv 0.96 1
rs10747050 1.000 0.040 9 137161424 splice region variant G/A snv 0.94 0.95 1
rs643410 1.000 0.040 9 109037283 intron variant A/C snv 0.93 1
rs2104425 0.925 0.040 6 40277470 upstream gene variant T/C snv 0.91 4
rs2486001 1.000 0.040 1 44010315 non coding transcript exon variant T/C snv 0.87 1
rs2255349 1.000 0.040 9 88201419 intergenic variant A/G snv 0.87 1
rs2710322 1.000 0.040 3 52783577 intron variant T/C snv 0.87 1
rs2440390 1.000 0.040 11 113416156 intron variant T/C snv 0.87 1
rs2518823 1.000 0.040 22 19972665 intron variant T/C snv 0.86 1
rs1355095 1.000 0.040 5 131913076 intron variant C/T snv 0.86 1
rs7713886 1.000 0.040 5 148645595 non coding transcript exon variant C/T snv 0.85 1
rs4234898 1.000 0.040 4 156077389 intergenic variant T/C snv 0.85 1
rs1734907 0.925 0.080 7 100717894 upstream gene variant A/G snv 0.84 2
rs2270954 1.000 0.040 18 53530928 3 prime UTR variant A/C snv 0.84 1
rs1548359 1.000 0.040 22 19515751 intron variant G/C snv 0.84 1
rs6785 0.851 0.120 2 207603273 3 prime UTR variant A/G snv 0.84 4
rs2745557 0.807 0.200 1 186680089 intron variant A/G snv 0.83 6
rs6502097 0.882 0.040 17 82328303 5 prime UTR variant C/G snv 0.83 3
rs548181 0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 1
rs988748 0.882 0.120 11 27703198 intron variant C/G snv 0.83 3
rs2660304 0.925 0.120 1 98046571 non coding transcript exon variant G/T snv 0.83 2
rs7103411 0.752 0.160 11 27678578 intron variant C/T snv 0.82 12