Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs26232 0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs2561477 1.000 0.120 5 103273223 intron variant G/A snv 0.24 1
rs39984 1.000 0.120 5 103261591 intron variant G/T snv 0.30 1