Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs828618 0.925 0.160 3 98822789 intron variant G/A snv 0.28 0.22 2
rs2427827 1.000 0.120 1 159302021 intron variant T/C snv 0.65 2
rs1391371 0.925 0.160 6 32636021 intron variant A/C;T snv 2
rs7817 0.925 0.200 7 112475603 3 prime UTR variant C/G;T snv 2
rs113795008 1.000 0.120 11 192836 intron variant A/G snv 0.17 1
rs2280540 1.000 0.120 11 192997 intron variant G/A;C;T snv 1
rs338598 1.000 0.120 19 41195623 intron variant C/A;G;T snv 1
rs17718444 1.000 0.120 3 71450250 intron variant C/T snv 0.27 1
rs6543124 1.000 0.120 2 102370999 intron variant T/A snv 0.44 1