Source: INFERRED ×
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: rs199476107
rs199476107
CYTB ; ND5 ; ND6
2 0.925 0.200 MT 14453 missense variant G/A snv 0.800 1.000 0 2001 2001
dbSNP: rs267606894
rs267606894
CYTB ; ND5
1 1.000 0.200 MT 12770 missense variant A/G snv 0.800 1.000 0 1997 2007
dbSNP: rs267606895
rs267606895
CYTB ; ND5
3 0.882 0.240 MT 13045 missense variant A/C snv 0.800 1.000 0 1997 2007
dbSNP: rs267606897
rs267606897
CYTB ; ND5
4 0.882 0.200 MT 13513 missense variant G/A snv 0.800 1.000 0 1997 2007
dbSNP: rs267606898
rs267606898
CYTB ; ND5
4 0.851 0.240 MT 13042 missense variant G/A snv 0.800 1.000 0 1997 2007
dbSNP: rs121434462
rs121434462
ND4 ; ND5 ; TRNL2
2 0.925 0.200 MT 12315 non coding transcript exon variant G/A snv 0.700 1.000 5 1996 2009
dbSNP: rs121434474
rs121434474
ND4 ; ND5 ; TRNH
2 0.925 0.200 MT 12147 non coding transcript exon variant G/A snv 0.700 1.000 2 2004 2004
dbSNP: rs267606896
rs267606896
CYTB ; ND5
2 0.882 0.200 MT 13084 missense variant A/T snv 0.700 0