Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1801131 0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11540652 0.592 0.640 17 7674220 missense variant C/A;G;T snv 1.2E-05 57
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs531564 0.672 0.480 8 9903189 non coding transcript exon variant G/C snv 0.14 27
rs2333227
MPO
0.752 0.320 17 58281401 upstream gene variant C/T snv 0.24 15
rs1332018 0.882 0.200 1 109740350 5 prime UTR variant G/T snv 0.64 0.66 6