Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs267606896
CYTB ; ND5
0.882 0.200 MT 13084 missense variant A/T snv 1
rs267606894
CYTB ; ND5
1.000 0.200 MT 12770 missense variant A/G snv 1
rs267606898
CYTB ; ND5
0.851 0.240 MT 13042 missense variant G/A snv 1
rs267606897
CYTB ; ND5
0.882 0.200 MT 13513 missense variant G/A snv 1
rs267606895
CYTB ; ND5
0.882 0.240 MT 13045 missense variant A/C snv 1
rs397515506
CYTB ; ND5 ; ND6
1.000 0.160 MT 14568 missense variant C/T snv 1
rs28359178
CYTB ; ND5 ; ND6
0.882 0.280 MT 13708 missense variant G/A snv 1
rs387906425
CYTB ; ND6 ; ND5
1.000 0.160 MT 13730 missense variant G/A snv 1
rs193302933
ND4 ; ND3 ; ND5 ; ND4L
1.000 0.160 MT 10664 synonymous variant C/T snv 1
rs199476112
ND4 ; ND5
0.925 0.160 MT 11778 missense variant G/A snv 1
rs200873900
ND4 ; ND5
1.000 0.200 MT 11696 missense variant G/A snv 1
rs267606893
ND5
0.925 0.120 MT 12706 missense variant T/C snv 1
rs267606899
ND5 ; CYTB
1.000 0.160 MT 12848 missense variant C/T snv 1
rs869025186
ND5 ; CYTB ; ND6
1.000 0.160 MT 14498 missense variant T/C snv 1
rs199476105
ND5 ; CYTB ; ND6
0.851 0.200 MT 14459 missense variant G/A snv 1
rs199476113
ND5 ; ND4 ; ND4L
1.000 0.200 MT 11084 missense variant A/G snv 1
rs267606892
ND5 ; ND4 ; ND4L ; ND3
1.000 0.080 MT 10563 missense variant T/C snv 1
rs199476107
ND5 ; ND6 ; CYTB
0.925 0.200 MT 14453 missense variant G/A snv 1
rs199476106
ND5 ; ND6 ; CYTB
1.000 0.160 MT 14495 missense variant A/G snv 1
rs199476109
ND6 ; CYTB ; ND5
0.882 0.120 MT 14487 missense variant T/C snv 1
rs199476104
ND6 ; CYTB ; ND5
0.925 0.160 MT 14484 missense variant T/C snv 1
rs199476108
ND6 ; CYTB ; ND5
1.000 0.160 MT 14482 missense variant C/A;G snv 1
rs387906424
ND6 ; ND5 ; CYTB
0.925 0.200 MT 14596 missense variant A/T snv 1