Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs564398 0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 7
rs10116277 0.827 0.160 9 22081398 intron variant G/T snv 0.62 5
rs523096 0.827 0.080 9 22019130 intron variant A/G snv 0.30 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
rs10811650 0.882 0.200 9 22067594 intron variant A/G snv 0.37 4
rs1333042 0.827 0.120 9 22103814 intron variant A/G snv 0.63 4
rs1333046 0.925 0.080 9 22124124 intron variant T/A snv 0.43 4
rs1537375 0.882 0.120 9 22116072 intron variant T/C;G snv 4
rs9632884 0.851 0.160 9 22072302 intron variant G/A;C snv 4
rs10738604 1.000 0.040 9 22025494 intron variant G/A snv 0.29 3
rs10738609 1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs10738610 0.882 0.120 9 22123767 intron variant A/C;T snv 3
rs10757269 1.000 0.040 9 22072265 intron variant A/C;G snv 3
rs10811647 1.000 0.040 9 22065003 intron variant C/G;T snv 3
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 3
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 3
rs3218020 0.882 0.120 9 21997873 intron variant G/A;C snv 3
rs615552 0.925 0.120 9 22026078 intron variant T/C snv 0.29 3
rs1004638 1.000 0.040 9 22115590 intron variant A/C;T snv 2
rs10511701 9 22112600 intron variant T/A;C snv 2
rs10733376 1.000 0.080 9 22114470 intron variant G/C snv 0.64 2
rs10811644 1.000 0.040 9 22025068 intron variant A/T snv 0.56 2
rs1333043 9 22106732 intron variant T/A snv 0.64 2