Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34