Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs729147 0.882 0.080 4 99412110 downstream gene variant G/A snv 0.78 3
rs2979704 0.827 0.200 8 24951554 3 prime UTR variant C/T snv 0.78 5
rs10055201 0.882 0.080 5 55865274 intron variant A/G snv 0.76 3
rs17489363 0.882 0.080 2 214809617 5 prime UTR variant A/G snv 0.73 0.74 3
rs3768707 0.882 0.080 2 214780411 intron variant A/G snv 0.74 3
rs391957 0.763 0.240 9 125241745 non coding transcript exon variant T/C snv 0.72 10
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs34330 0.724 0.280 12 12717761 5 prime UTR variant T/C snv 0.70 15
rs11994014 0.827 0.200 8 24944767 intergenic variant A/G snv 0.70 5
rs4796030 0.827 0.120 17 35003131 3 prime UTR variant A/C snv 0.66 6
rs238406 0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs6939340 0.851 0.160 6 22139775 intron variant A/G snv 0.62 4
rs1501899 0.790 0.240 3 122188481 intron variant A/G snv 0.62 8
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs873601 0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs9295536 0.882 0.080 6 22131700 intron variant C/A snv 0.58 3
rs514049 0.827 0.160 15 58750164 intron variant C/A snv 0.57 6
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs9653226 0.882 0.080 2 15939632 intron variant C/T snv 0.54 3
rs221634 0.851 0.080 6 105080213 3 prime UTR variant T/A snv 0.52 4
rs1027702 0.882 0.080 1 161743067 intergenic variant C/T snv 0.51 3
rs6441201 0.882 0.080 3 158460535 intron variant G/A snv 0.51 3
rs3788266 0.732 0.160 21 46606442 upstream gene variant G/A snv 0.50 12
rs10840002 0.882 0.080 11 8221479 downstream gene variant A/G snv 0.49 3