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 15
rs61839660 0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs2104286 0.662 0.440 10 6057082 intron variant T/C snv 0.18 7
rs3118470 0.752 0.360 10 6059750 intron variant T/A;C snv 2
rs12722495 0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 1