Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199476133 0.692 0.214 MT 8993 missense variant snp 15
rs113994098 0.692 0.286 15 89321792 missense variant C/T snp 1.5E-04 3.5E-04 10
rs267606891
ND3
0.744 0.179 MT 10197 missense variant snp 9
rs267606893
ND5
0.756 0.107 MT 12706 missense variant snp 9
rs199476135 0.769 0.107 MT 9176 missense variant snp 8
rs28939711 0.756 0.107 10 99724057 stop gained G/A snp 3.2E-05 8
rs759452074 0.769 0.179 22 50523835 missense variant C/A,T snp 8.0E-06; 3.2E-05 8
rs199476138 0.769 0.107 MT 9185 missense variant snp 7
rs397514662 0.769 0.107 10 99716419 stop lost A/C,G snp 1.2E-05 7
rs121912638 0.784 0.107 11 68033216 missense variant G/A snp 2.0E-05 7
rs28939679 0.769 0.107 11 68033147 missense variant C/T snp 8.1E-06 7
rs267606896
ND5
0.769 0.179 MT 13084 missense variant snp 7
rs387906873 0.784 0.107 2 240021232 missense variant T/C snp 7
rs199592341 0.784 0.107 12 4685324 missense variant G/A,C,T snp 3.6E-05; 4.0E-06 3.2E-05 7
rs267606689 0.769 0.107 20 13794939 missense variant A/C snp 7
rs757043077 0.769 0.107 20 13808873 missense variant G/T snp 4.0E-06; 4.4E-05 7
rs747359752 0.784 0.107 5 53658555 missense variant G/C snp 8.0E-06 7
rs121913659 0.769 0.107 11 67612225 missense variant C/T snp 1.2E-05 7
rs113994093 0.784 0.107 15 89330241 missense variant C/T snp 1.2E-05 7
rs137852767 0.784 0.107 5 251011 missense variant C/T snp 7
rs9809219 0.784 0.107 5 251100 missense variant C/T snp 4.0E-05 7
rs121918658 0.784 0.107 9 133352074 missense variant A/C snp 7
rs28933402 0.784 0.107 9 133353893 missense variant C/T snp 7
rs398122806 0.784 0.107 9 133352518 missense variant A/G snp 7
rs782033035 0.784 0.107 9 133353894 missense variant C/T snp 1.2E-05 7