Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs7574865 0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 22
rs548234 0.763 0.360 6 106120159 intron variant C/T snv 0.76 11