Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs1047972 0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs587779157 0.827 0.240 2 47408486 inframe deletion GAAGTT/- delins 6
rs142155101 0.925 0.120 2 214728728 missense variant C/T snv 1.7E-03 1.5E-03 3