Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs706778 0.695 0.320 10 6056986 intron variant C/T snv 0.46 4
rs12722489 0.882 0.160 10 6060049 intron variant C/T snv 0.11 2
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 2
rs3118470 0.752 0.360 10 6059750 intron variant T/A;C snv 2