Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1799969 0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs7517847 0.689 0.600 1 67215986 intron variant T/G snv 0.37 19
rs1893217 0.742 0.440 18 12809341 intron variant A/G snv 0.12 14
rs3024490 0.742 0.520 1 206771966 intron variant A/C;G;T snv 11
rs11209032 0.752 0.400 1 67274409 upstream gene variant G/A snv 0.30 10
rs1048709 0.776 0.320 6 31947158 synonymous variant A/G snv 0.82 0.85 8
rs4505848 0.776 0.400 4 122211337 intron variant A/G snv 0.29 8
rs17375018 0.790 0.360 1 67189464 intron variant G/A snv 0.29 7
rs10863888 0.851 0.280 1 211329427 intron variant A/C;G;T snv 4
rs12569232 0.882 0.280 1 211379722 intron variant G/C;T snv 4
rs1805110 0.882 0.200 1 91861488 missense variant G/A snv 0.13 0.13 3
rs2489188 0.925 0.200 1 91866932 intron variant C/T snv 0.65 2