Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2534657 0.882 0.200 6 31504682 intron variant C/T snv 0.15 6
rs2534678 0.925 0.120 6 31496186 intron variant G/A;T snv 5
rs3134899 1.000 6 31505509 intron variant C/T snv 0.80 4
rs3828917 1.000 6 31498140 5 prime UTR variant G/A;T snv 4
rs3095234 1.000 6 31496794 intron variant C/A;T snv 4