Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs281432 0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs5491 0.827 0.160 19 10274864 missense variant A/G;T snv 4.0E-06; 2.8E-02 6