Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1406948 20 35317816 intron variant G/A snv 0.44 2
rs4911180 20 35385145 intron variant G/A snv 0.54 1
rs4911492 20 35363996 intron variant G/A;C snv 1