Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1029388 12 111489097 intron variant T/C snv 0.38 1
rs616559 12 111565546 intron variant T/C snv 0.31 1
rs6490162 12 111503316 intron variant T/C snv 0.32 1