Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1556425596 0.752 0.240 21 45989967 intron variant C/T snv 37
rs543860009 0.742 0.320 2 178589003 stop gained G/A;T snv 33
rs878854378 0.742 0.320 2 178533657 inframe deletion GTT/- delins 33
rs121908557 0.752 0.280 17 63957514 missense variant C/T snv 8.2E-06 1.4E-05 19
rs912001256 0.851 0.240 17 63947062 stop gained G/A snv 17