Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1801278 0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs1799782 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 151
rs4684677 0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101