Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs471364 1.000 0.040 9 15289580 intron variant C/T snv 0.87 3
rs581080 9 15305380 intron variant G/C snv 0.72 3
rs643531 9 15296036 intron variant C/A snv 0.89 2