Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs10506868 0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs11196172 0.708 0.200 10 112967084 intron variant G/A snv 0.13 18
rs12241008 0.716 0.160 10 112520943 intron variant T/C snv 0.13 16
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93