Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6214 0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs1520220 0.807 0.280 12 102402744 intron variant G/C;T snv 0.76 9
rs7136446 0.882 0.160 12 102444737 intron variant C/T snv 0.66 8
rs6220 0.925 0.080 12 102400737 3 prime UTR variant G/A snv 0.67 4
rs1239905891 0.925 0.080 12 102475786 missense variant G/A;T snv 3