Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004638 1.000 0.040 9 22115590 intron variant A/C;T snv 3
rs10116277 0.827 0.160 9 22081398 intron variant G/T snv 0.62 8
rs10738607 0.925 0.080 9 22088095 intron variant A/G snv 0.42 4
rs10738610 0.882 0.120 9 22123767 intron variant A/C;T snv 5
rs10757264 1.000 0.040 9 22019733 intron variant A/G snv 0.58 2
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10811656 0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs10965212 0.925 0.080 9 22023796 intron variant T/A;C;G snv 3
rs10965215 0.882 0.120 9 22029446 missense variant G/A snv 0.55 0.46 4
rs10965219 0.882 0.080 9 22053688 intron variant A/G snv 0.58 4
rs1333040 0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs1333042 0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs1333047 0.790 0.240 9 22124505 intron variant A/T snv 0.63 9
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs1537372 0.752 0.120 9 22103184 intron variant G/A;T snv 14
rs1537374 1.000 0.040 9 22116047 intron variant A/G snv 0.64 3
rs1537375 0.882 0.120 9 22116072 intron variant T/C;G snv 6
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs2026458 0.882 0.080 6 12825642 intron variant C/T snv 0.34 6
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22