Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2228145 0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs2229113 0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs2231142 0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4684677 0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 13
rs5498 0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs878854066 0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs281864525
HBB
0.851 0.280 11 5227097 5 prime UTR variant T/A;G snv 7.0E-06 4
rs34166473
HBD
0.827 0.320 11 5234513 5 prime UTR variant A/G snv 7.0E-06 6
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs63750953
HBB
0.790 0.400 11 5227097 5 prime UTR variant TT/- delins 7.0E-06 10
rs6198 0.724 0.480 5 143278056 3 prime UTR variant T/C snv 0.12 16
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1799724
LTA ; TNF
0.600 0.680 6 31574705 upstream gene variant C/T snv 8.5E-02 47
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs361525
TNF
0.562 0.760 6 31575324 upstream gene variant G/A snv 4.6E-02 62
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17