Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6822844 0.689 0.520 4 122588266 regulatory region variant G/T snv 0.10 20
rs6920220 0.742 0.440 6 137685367 intron variant G/A snv 0.16 14
rs6932542 0.827 0.200 6 32412485 downstream gene variant A/G snv 0.55 5
rs729302 0.827 0.160 7 128928906 intergenic variant A/C snv 0.28 6
rs744600 0.851 0.160 2 190700031 intron variant G/T snv 0.60 4
rs7579944 0.882 0.200 2 30222160 intergenic variant T/C;G snv 5
rs7745656 0.882 0.200 6 32713193 upstream gene variant G/T snv 0.29 3
rs7758736 0.882 0.200 6 32790617 intergenic variant G/A snv 0.14 3
rs7762279 0.807 0.360 6 32787513 intergenic variant T/C snv 8.4E-02 6
rs7929541 0.851 0.160 11 633689 upstream gene variant T/C snv 0.34 4
rs906868 0.925 0.120 2 30225478 intergenic variant G/T snv 0.53 4
rs9271366 0.807 0.240 6 32619077 intergenic variant G/A snv 0.86 9
rs9275141 0.827 0.240 6 32683340 intergenic variant T/G snv 0.50 6
rs9275328 0.851 0.240 6 32699045 intergenic variant C/T snv 0.16 4
rs9275428 0.925 0.120 6 32703201 downstream gene variant A/C;G snv 2
rs9275572 0.724 0.360 6 32711222 upstream gene variant A/G;T snv 15
rs9357152 0.827 0.240 6 32697183 regulatory region variant A/G snv 0.24 5
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1800682 0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs340630 0.925 0.120 4 87037243 intron variant G/A snv 0.42 2
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2075876 0.925 0.120 21 44289270 non coding transcript exon variant G/A snv 0.19 2
rs878081 0.882 0.200 21 44288394 synonymous variant C/T snv 0.21 0.19 3
rs7731626 0.716 0.240 5 56148856 intron variant G/A snv 0.30 16
rs1217393 0.851 0.160 1 113891324 intron variant G/A snv 0.42 4