Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8095142 18 46213842 intron variant G/A snv 0.64 2
rs6507691 18 46228682 intron variant T/C;G snv 1
rs8095374 18 46213522 intron variant T/C snv 0.43 1