Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs6993770 0.925 0.080 8 105569300 intron variant A/T snv 0.31 9
rs28357984
ND2 ; COX1
0.851 0.160 MT 5178 missense variant C/A snv 6
rs752596535 0.752 0.200 19 11105407 stop gained C/A;G;T snv 1.6E-05 14
rs33972313 0.790 0.160 5 139379813 missense variant C/A;G;T snv 4.0E-06; 2.7E-02 8
rs5742904 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs1800206 0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1799895 0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs11053646 0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs2735383 0.708 0.360 8 89935041 3 prime UTR variant C/G snv 0.31 18
rs138880920 1.000 0.040 9 104826957 missense variant C/G snv 3.3E-03 1.8E-03 1
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1764391 0.790 0.160 1 34795168 missense variant C/G;T snv 0.30 7
rs2066718 0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 7
rs2375981 1.000 0.040 9 2692583 regulatory region variant C/G;T snv 2
rs750249283 0.925 0.080 21 42296256 missense variant C/G;T snv 4.0E-06; 8.0E-06 2
rs33918808 1.000 0.040 9 104817351 missense variant C/G;T snv 3.5E-02; 4.0E-06 1
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182