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: rs267606894
rs267606894
CYTB ; ND5
1 1.000 0.200 MT 12770 missense variant A/G snv 0.800 1.000 4 1997 2007
dbSNP: rs267606895
rs267606895
CYTB ; ND5
3 0.882 0.240 MT 13045 missense variant A/C snv 0.800 1.000 4 1997 2007
dbSNP: rs267606897
rs267606897
CYTB ; ND5
4 0.882 0.200 MT 13513 missense variant G/A snv 0.800 1.000 4 1997 2007
dbSNP: rs267606898
rs267606898
CYTB ; ND5
4 0.851 0.240 MT 13042 missense variant G/A snv 0.800 1.000 4 1997 2007
dbSNP: rs199476107
rs199476107
CYTB ; ND5 ; ND6
2 0.925 0.200 MT 14453 missense variant G/A snv 0.800 1.000 1 2001 2001
dbSNP: rs199474701
rs199474701
CYTB ; ND6 ; TRNP
3 0.925 0.200 MT 15967 non coding transcript exon variant G/A snv 0.700 1.000 2 2009 2009
dbSNP: rs121434453
rs121434453
CYTB ; ND6 ; TRNE
4 0.882 0.320 MT 14709 non coding transcript exon variant T/C snv 0.700 1.000 1 1995 1995
dbSNP: rs387906421
rs387906421
CYTB ; ND6 ; TRNE
3 0.925 0.200 MT 14674 non coding transcript exon variant T/C;G snv 0.700 1.000 1 2009 2009
dbSNP: rs267606896
rs267606896
CYTB ; ND5
3 0.882 0.200 MT 13084 missense variant A/T snv 0.700 0