Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2642438 1 220796686 missense variant A/G snv 0.75 0.78 6
rs1874124 1 220801995 intron variant C/T snv 0.11 2
rs2642442 1 220800221 intron variant C/T snv 0.73 2
rs2807834 1 220797251 intron variant T/C;G snv 2