Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2275913 0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs763110 0.653 0.560 1 172658358 upstream gene variant C/T snv 0.49 30
rs1143633 0.752 0.280 2 112832890 intron variant C/G;T snv 11