Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs36001488 0.724 0.240 2 233276621 intron variant C/T snv 0.44 14
rs35300242 0.827 0.120 2 233260144 intron variant G/A;C snv 5
rs2241880 0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 1