Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs10401969 0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs4803750 0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs673548 0.925 0.120 2 21014672 intron variant G/A;T snv 14
rs2650000 0.851 0.200 12 120951159 intron variant A/C snv 0.70 10