Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10487818 1.000 0.080 7 106269615 intron variant A/T snv 1.1E-02 1
rs1064891 0.925 0.080 10 6234611 3 prime UTR variant T/C snv 0.37 2
rs121913564 0.882 0.080 18 60371403 missense variant A/C snv 2.0E-05 1.4E-05 3
rs121913566 0.925 0.080 18 60372165 missense variant T/C snv 4.0E-06 2
rs12510549 0.882 0.160 4 10274843 intergenic variant T/C snv 0.18 4
rs1322837244 0.925 0.080 19 45698622 missense variant C/T snv 2
rs13447331 0.925 0.080 18 60371970 missense variant G/A snv 1.7E-04 7.7E-05 2
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1800571 0.925 0.080 3 12381349 missense variant C/A snv 1.4E-05 2
rs1800949 1.000 0.080 6 131807424 upstream gene variant C/G;T snv 0.18 1
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805096 0.827 0.200 1 65636574 synonymous variant G/A snv 0.46 0.43 6
rs1805097 0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1805134 0.925 0.160 1 65601426 synonymous variant T/C snv 0.22 0.24 2
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs199951903
ND6 ; CYTB
0.925 0.120 MT 15497 missense variant G/A snv 2
rs201408477 0.925 0.080 2 25161455 missense variant A/G snv 1.8E-04 1.6E-04 2
rs2076349 0.882 0.120 1 209626885 missense variant C/T snv 0.13 0.13 3
rs2229616 0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 22
rs2239607 0.925 0.120 12 109209475 intron variant A/G snv 0.14 3
rs2268388 0.851 0.200 12 109205840 intron variant G/A snv 0.14 6
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs35859249 0.807 0.200 4 37902468 missense variant C/A;T snv 4.0E-06; 9.7E-02 6
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41