Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1537375 0.882 0.120 9 22116072 intron variant T/C;G snv 6
rs2026458 0.882 0.080 6 12825642 intron variant C/T snv 0.34 6
rs217181 16 72080103 intron variant C/T snv 0.20 6
rs2383204 0.827 0.160 9 22055049 intron variant A/G;T snv 6
rs2731672 5 177415473 intron variant T/C snv 0.66 6
rs496892 0.827 0.160 9 22024352 intron variant C/T snv 0.40 6
rs634537 0.851 0.080 9 22032153 intron variant T/G snv 0.28 6
rs9632884 0.851 0.160 9 22072302 intron variant G/A;C snv 6
rs10738610 0.882 0.120 9 22123767 intron variant A/C;T snv 5
rs10811650 0.882 0.200 9 22067594 intron variant A/G snv 0.37 5
rs2891168 0.851 0.160 9 22098620 intron variant A/G snv 0.40 5
rs3218020 0.882 0.120 9 21997873 intron variant G/A;C snv 5
rs6475606 0.882 0.080 9 22081851 intron variant C/T snv 0.62 5
rs944797 0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 5
rs10127775 1 230160042 intron variant A/G;T snv 4
rs10211524 2 64980940 intron variant G/A snv 0.51 4
rs10738607 0.925 0.080 9 22088095 intron variant A/G snv 0.42 4
rs10757269 1.000 0.040 9 22072265 intron variant A/C;G snv 4
rs10965219 0.882 0.080 9 22053688 intron variant A/G snv 0.58 4
rs1333046 0.925 0.080 9 22124124 intron variant T/A snv 0.43 4
rs1440581 1.000 0.080 4 88305270 intron variant T/A;C snv 4
rs1537378 0.882 0.160 9 22061615 intron variant A/G snv 0.73 4
rs1912826 4 186228386 intron variant G/A;C snv 4
rs615552 0.925 0.120 9 22026078 intron variant T/C snv 0.29 4
rs944801 0.882 0.120 9 22051671 intron variant G/A;C snv 4