Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs139401390 0.851 0.120 10 88643382 regulatory region variant A/G snv 1.0E-02 5
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2576178 0.790 0.160 10 88583641 5 prime UTR variant A/G snv 0.29 9
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3834458 0.807 0.200 11 61827449 intron variant T/- del 0.28 7
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs911119 0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs767830104 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs995922697 0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs4961 0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs3746444 0.514 0.760 20 34990448 mature miRNA variant A/G snv 0.20 0.19 105
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38