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: rs267606895
rs267606895
CYTB ; ND5
3 0.882 0.240 MT 13045 missense variant A/C snv 0.700 0
dbSNP: rs267606896
rs267606896
CYTB ; ND5
3 0.882 0.200 MT 13084 missense variant A/T snv 0.700 0
dbSNP: rs199476105
rs199476105
CYTB ; ND5 ; ND6
4 0.851 0.200 MT 14459 missense variant G/A snv 0.700 0
dbSNP: rs267606897
rs267606897
CYTB ; ND5
4 0.882 0.200 MT 13513 missense variant G/A snv 0.700 0
dbSNP: rs267606898
rs267606898
CYTB ; ND5
4 0.851 0.240 MT 13042 missense variant G/A snv 0.700 0
dbSNP: rs199476109
rs199476109
CYTB ; ND5 ; ND6
3 0.882 0.120 MT 14487 missense variant T/C snv 0.700 0
dbSNP: rs267606889
rs267606889
COX1 ; ND1 ; ND2
2 0.925 0.120 MT 4681 missense variant T/C snv 0.700 0
dbSNP: rs267606893
rs267606893
ND5
2 0.925 0.120 MT 12706 missense variant T/C snv 0.700 0