Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2082940 0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv 10
rs5030772 0.790 0.320 1 172664210 intron variant A/G snv 9.9E-02 7
rs7775228 0.790 0.360 6 32690302 TF binding site variant T/C snv 0.15 7
rs2929970 0.827 0.200 8 133228894 3 prime UTR variant G/A snv 0.52 5
rs7135617 0.827 0.240 12 121631099 intron variant T/C;G snv 5
rs2289263 0.925 0.120 15 67146869 intron variant T/G snv 0.43 3
rs3219463 0.925 0.120 1 45340760 5 prime UTR variant C/T snv 0.27 2
rs6494629 0.925 0.120 15 67081773 intron variant C/T snv 0.52 2