Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9268402 0.827 0.200 6 32373576 intron variant G/A snv 0.45 4
rs6910071 0.790 0.320 6 32315077 intron variant A/G snv 0.14 3
rs9268403 0.807 0.240 6 32373696 intron variant T/C snv 0.24 3
rs9268145 0.925 0.160 6 32289507 intron variant T/G snv 0.14 2
rs9268362 0.925 0.160 6 32365564 intron variant A/G snv 0.16 0.15 2
rs28366178 1.000 0.040 6 32308498 intron variant T/C snv 0.14 1
rs9268400 1.000 0.040 6 32372877 intron variant G/A snv 0.24 1
rs2281276 1.000 0.040 6 32372329 intron variant A/G snv 0.41 1
rs28361060 1.000 0.040 6 32336071 intron variant G/A snv 0.14 1
rs6913309 1.000 0.040 6 32372063 intron variant T/A snv 0.27 1
rs9268401 1.000 0.040 6 32373541 intron variant A/G snv 0.24 1