Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6983267 0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 55
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 17
rs7837328 0.882 0.120 8 127410882 intron variant A/G snv 0.52 8
rs7014346 0.732 0.240 8 127412547 intron variant A/G snv 0.63 5
rs10505474 0.925 0.080 8 127405259 intron variant T/C snv 0.47 3
rs620861 0.925 0.080 8 127323428 intron variant G/A snv 0.36 2