Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6119267 20 32576112 intron variant C/A;G snv 3
rs12480732 20 32603213 intron variant C/T snv 0.19 2
rs7266642 20 32593666 intron variant A/G snv 0.50 1
rs67696533 20 32585560 intron variant G/A;T snv 1