Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10936599 0.637 0.600 3 169774313 synonymous variant C/T snv 0.29 0.21 15
rs140522 0.851 0.160 22 50532837 upstream gene variant T/A;C snv 10
rs11755724 0.807 0.320 6 7118757 intron variant A/G;T snv 5
rs6793295 0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 5
rs2777899 0.851 0.160 17 59755030 intron variant T/A;G snv 4
rs802734 0.827 0.280 6 127957653 intergenic variant A/G;T snv 4
rs806321 0.851 0.160 13 50267187 intron variant C/T snv 0.47 4
rs1292034 0.882 0.160 17 59912499 intron variant G/A snv 0.56 3