Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6725887 0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 4
rs3731695 2 202955552 intron variant T/C snv 0.46 1
rs11691351 2 203009189 intron variant A/G snv 0.42 1
rs3845802 2 202875949 3 prime UTR variant T/G snv 0.42 1
rs3933629 2 202901644 intron variant T/C snv 0.39 1
rs17406900 2 202919479 intron variant A/G snv 0.42 1