Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2249825 0.695 0.440 13 30463766 5 prime UTR variant G/A;C;T snv 23
rs767649 0.695 0.480 21 25572410 intron variant T/A snv 7.5E-02 18
rs1412125 0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1360485 0.742 0.320 13 30457747 3 prime UTR variant C/T snv 0.58 16
rs2229080
DCC
0.742 0.320 18 52906232 missense variant C/A;G snv 0.45 16
rs2221903 0.752 0.360 4 122617757 intron variant C/T snv 0.77 12
rs77191406 0.790 0.280 6 137881704 3 prime UTR variant C/T snv 7.2E-04 12
rs3219175 0.807 0.240 19 7668969 upstream gene variant G/A snv 5.0E-02 10