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
rs1555377415 0.827 0.200 14 77027274 stop gained G/C snv 18