Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs61755320 0.716 0.520 16 89546737 missense variant C/T snv 2.9E-03 3.5E-03 41
rs1556425596 0.752 0.240 21 45989967 intron variant C/T snv 37
rs1555358382 14 54844115 stop gained G/A snv 6