Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs57457691 19 33420799 intron variant T/C snv 0.62 3
rs731839 19 33408159 intron variant G/A snv 0.63 3
rs12460070 19 33442547 intron variant T/A;C snv 1