Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11203203 0.807 0.240 21 42416077 intron variant G/A snv 0.28 5
rs1893592 0.742 0.280 21 42434957 missense variant A/C;G snv 0.27; 8.0E-06 2
rs3788013 0.851 0.240 21 42421219 intron variant C/A snv 0.44 1