Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs207459995
CYTB ; ND6
1.000 0.080 MT 14985 missense variant G/A snv 1
rs200336777
CYTB ; ND6
1.000 0.160 MT 15812 missense variant G/A snv 1
rs387906425
CYTB ; ND6 ; ND5
1.000 0.160 MT 13730 missense variant G/A 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
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
rs207459996
ND6 ; CYTB
1.000 0.080 MT 15572 missense variant T/C snv 1
rs41518645
ND6 ; CYTB
0.925 0.200 MT 15257 missense variant G/A snv 1
rs207460003
ND6 ; CYTB
1.000 0.040 MT 15498 missense variant G/A 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