Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2222543 7 121262131 intron variant G/C snv 0.38 1
rs4731009 7 121264763 intron variant C/T snv 0.38 1
rs6942652 7 121249218 intron variant G/C;T snv 1