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
rs7708392 0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs7582694 0.763 0.400 2 191105394 intron variant C/G snv 0.77 9