Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 30
rs3800373 0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs9296158 0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs4713916 0.790 0.160 6 35702206 intron variant A/C;G;T snv 11
rs9394309 0.851 0.040 6 35654004 intron variant G/A snv 0.74 4