Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53