Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 8
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 7
rs212388 0.827 0.240 6 159069404 intron variant C/G;T snv 4
rs657555 0.925 0.080 18 12847137 intron variant C/A;T snv 3