Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11031006 0.882 0.120 11 30204981 intron variant G/A snv 0.11 8
rs12294104 11 30361352 intergenic variant C/T snv 0.14 4
rs56949836 1.000 0.120 9 90167763 intergenic variant C/T snv 8.9E-02 2
rs76169311 1.000 0.120 1 197372771 intron variant G/A snv 0.13 2
rs11031002 11 30193714 intron variant T/A snv 0.10 2