Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2187668 0.701 0.480 6 32638107 intron variant C/T snv 3.3E-03 11
rs9272346 0.790 0.320 6 32636595 intron variant G/A snv 0.54 4
rs146668528 1.000 0.080 6 32630251 intron variant C/T snv 5.7E-02 2
rs17843604 0.925 0.120 6 32652506 intergenic variant C/T snv 0.49 1
rs28798705 1.000 0.080 6 32650032 downstream gene variant A/G snv 0.66 1
rs3104367 1.000 0.080 6 32635710 intron variant T/C snv 0.57 1
rs9273123 1.000 0.080 6 32644956 non coding transcript exon variant G/A snv 0.46 1
rs28383364 1.000 0.080 6 32639135 3 prime UTR variant A/G snv 0.11 1
rs28383454 1.000 0.080 6 32641593 intron variant G/C;T snv 3.2E-03 1