Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs4810485 0.732 0.480 20 46119308 intron variant T/A;G snv 16
rs9266150 0.925 0.040 6 31356368 missense variant A/C;G;T snv 0.12; 7.9E-05; 3.8E-04 3