Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12443621 0.807 0.120 16 52514125 intron variant A/G snv 0.48 6
rs1123428 0.925 0.080 16 52543923 intron variant T/A snv 0.51 2
rs1362548 0.925 0.080 16 52530039 intron variant G/C;T snv 2
rs1420546 0.925 0.080 16 52454795 intron variant C/A;T snv 2
rs8051542 0.925 0.080 16 52500255 intron variant T/C snv 0.61 2