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
rs199476105
ND6
0.801 0.179 MT 14459 missense variant snp 3
rs104894885 0.801 0.143 X 119873312 missense variant G/A,C snp 2
rs267606897
ND5
0.821 0.179 MT 13513 missense variant snp 3
rs104894884 0.821 0.107 X 119871933 missense variant G/C 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
rs104894705 0.846 0.107 19 1391006 missense variant G/A snp 5.6E-05 6.4E-05 2
rs199476109
ND6
0.846 0.107 MT 14487 missense variant snp 2
rs199476117
ND3
0.846 0.107 MT 10158 missense variant snp 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
rs199476123
ND1
0.878 0.179 MT 3946 missense variant snp 2
rs267606890
ND3
0.878 0.107 MT 10191 missense variant snp 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
rs118203929 0.923 0.036 20 13801652 missense variant T/C snp 2.0E-05 2
rs121434427 0.923 0.036 1 161209912 missense variant G/A snp 2
rs121434428 0.923 0.036 1 161209915 missense variant C/A snp 2
rs121434429 0.923 0.036 1 161213673 missense variant T/C snp 2
rs121913660 0.923 0.036 11 67611511 missense variant C/T snp 3.2E-05 3.2E-05 2
rs121913661 0.923 0.036 11 67610510 missense variant G/A snp 3.2E-05 2