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
rs1043679457 0.752 0.400 5 60927745 intron variant C/A;G;T snv 33
rs1554768245 0.807 0.160 6 152472395 frameshift variant C/- delins 16