Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs199476104
rs199476104
CYTB ; ND5 ; ND6
2 0.925 0.160 MT 14484 missense variant T/C snv 0.810 1.000 7 1992 2001
dbSNP: rs199476108
rs199476108
CYTB ; ND5 ; ND6
1 1.000 0.160 MT 14482 missense variant C/A;G snv 0.810 1.000 6 1992 2002
dbSNP: rs199476106
rs199476106
CYTB ; ND5 ; ND6
1 1.000 0.160 MT 14495 missense variant A/G snv 0.800 1.000 5 1992 2001
dbSNP: rs397515506
rs397515506
CYTB ; ND5 ; ND6
1 1.000 0.160 MT 14568 missense variant C/T snv 0.800 1.000 5 1992 2001
dbSNP: rs387906425
rs387906425
CYTB ; ND5 ; ND6
1 1.000 0.160 MT 13730 missense variant G/A snv 0.800 1.000 4 1991 2005
dbSNP: rs869025186
rs869025186
CYTB ; ND5 ; ND6
1 1.000 0.160 MT 14498 missense variant T/C snv 0.700 1.000 5 1992 2001
dbSNP: rs28359178
rs28359178
CYTB ; ND5 ; ND6
3 0.882 0.280 MT 13708 missense variant G/A snv 0.700 1.000 4 1991 2005
dbSNP: rs41518645
rs41518645
CYTB ; ND6
3 0.925 0.200 MT 15257 missense variant G/A snv 0.700 1.000 1 1992 1992
dbSNP: rs199476105
rs199476105
CYTB ; ND5 ; ND6
4 0.851 0.200 MT 14459 missense variant G/A snv 0.700 0
dbSNP: rs200336777
rs200336777
CYTB ; ND6
1 1.000 0.160 MT 15812 missense variant G/A snv 0.700 0
dbSNP: rs387906424
rs387906424
CYTB ; ND5 ; ND6
2 0.925 0.200 MT 14596 missense variant A/T snv 0.700 0