Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs657197 12 111527854 intron variant C/A;T snv 1
rs607316 12 111531644 intron variant C/T snv 0.31 1
rs616513 12 111565579 intron variant G/A;T snv 1