Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12914385 0.790 0.160 15 78606381 intron variant C/A;T snv 8
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 7
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 5
rs1062980 0.827 0.080 15 78500185 3 prime UTR variant T/C snv 0.39 4
rs13180 0.851 0.160 15 78497146 synonymous variant C/T snv 0.54 0.51 4
rs1903003 0.925 0.080 4 88965146 intron variant C/G;T snv 3