Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs138740 0.882 0.160 22 35303589 intron variant C/T snv 0.51 3
rs138747 1.000 0.160 22 35304495 intron variant A/C;T snv 1
rs138777 22 35315105 intron variant A/G snv 0.51 1
rs138788 1.000 0.040 22 35333728 intron variant G/A snv 0.49 1