Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17576 0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs243865 0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs1219648 0.716 0.320 10 121586676 intron variant A/G;T snv 17