Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59