Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs58141407 8 21934261 intron variant C/T snv 0.11 3
rs80207740 8 21922426 intron variant C/G snv 0.12 2
rs7843479 8 21963302 intron variant C/A;T snv 1