Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267606891
ND3
0.744 0.179 MT 10197 missense variant snp 9
rs267606893
ND5
0.756 0.107 MT 12706 missense variant snp 9
rs267606897
ND5
0.821 0.179 MT 13513 missense variant snp 3
rs199476105
ND6
0.801 0.179 MT 14459 missense variant snp 3
rs121918134 0.923 0.036 3 49022497 missense variant G/A,C snp 4.0E-06 2
rs267606830 0.923 0.036 11 126277517 missense variant A/C,G snp 4.0E-06 2
rs387907087 0.923 0.036 11 126276476 missense variant C/T snp 2.4E-05 6.4E-05 2
rs63751061 0.923 0.036 6 96896790 missense variant A/G snp 2
rs199476123
ND1
0.878 0.179 MT 3946 missense variant snp 2
rs199476117
ND3
0.846 0.107 MT 10158 missense variant snp 2
rs267606890
ND3
0.878 0.107 MT 10191 missense variant snp 2
rs267606895
ND5
0.821 0.214 MT 13045 missense variant snp 2
rs267606898
ND5
0.821 0.179 MT 13042 missense variant snp 2
rs199476109
ND6
0.846 0.107 MT 14487 missense variant snp 2
rs121918135 0.923 0.036 3 49022903 missense variant G/C snp 2
rs118203929 0.923 0.036 20 13801652 missense variant T/C snp 2.0E-05 2
rs1057519084 0.878 0.107 8 95032023 missense variant T/C snp 2
rs1057519085 0.878 0.107 8 95032003 missense variant A/T snp 2
rs1057519086 0.878 0.107 8 95052177 missense variant A/G snp 2
rs137853184 0.878 0.107 8 95032093 missense variant A/G snp 2
rs201732170 0.923 0.036 8 95035527 missense variant T/A,C snp 4.0E-06; 9.2E-05 3.2E-05 2
rs768273248 0.878 0.107 8 95048547 missense variant C/G,T snp 4.0E-06; 8.0E-06 2
rs1057519073 0.923 0.036 X 47142418 missense variant C/T snp 2
rs142609245 0.923 0.036 2 201078946 missense variant T/C snp 8.5E-04 8.0E-04 2
rs199422224 0.923 0.036 2 206145009 missense variant T/C snp 4.0E-06 2