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: rs193302996
rs193302996
CYTB ; ND6
1 1.000 0.120 MT 15607 synonymous variant A/G snv 0.700 0
dbSNP: rs193302997
rs193302997
CYTB ; ND6
1 1.000 0.120 MT 15670 synonymous variant T/C snv 0.700 0
dbSNP: rs527236161
rs527236161
CYTB ; ND6
1 1.000 0.120 MT 14743 upstream gene variant A/G snv 0.700 0
dbSNP: rs527236162
rs527236162
CYTB ; ND6
1 1.000 0.120 MT 14753 missense variant C/T snv 0.700 0
dbSNP: rs527236163
rs527236163
CYTB ; ND6
1 1.000 0.120 MT 14784 missense variant T/C snv 0.700 0
dbSNP: rs527236171
rs527236171
CYTB ; ND6
1 1.000 0.120 MT 15058 synonymous variant C/T snv 0.700 0
dbSNP: rs527236178
rs527236178
CYTB ; ND6
1 1.000 0.120 MT 15328 synonymous variant A/G snv 0.700 0
dbSNP: rs527236179
rs527236179
CYTB ; ND6
1 1.000 0.120 MT 15334 synonymous variant C/T snv 0.700 0
dbSNP: rs527236182
rs527236182
CYTB ; ND6
1 1.000 0.120 MT 15363 missense variant A/G snv 0.700 0
dbSNP: rs527236196
rs527236196
CYTB ; ND6 ; TRNT
1 1.000 0.120 MT 15890 non coding transcript exon variant C/A snv 0.700 0
dbSNP: rs527236199
rs527236199
CYTB ; ND6 ; TRNT
1 1.000 0.120 MT 15932 non coding transcript exon variant T/C;G snv 0.700 0
dbSNP: rs527236205
rs527236205
CYTB ; ND6
1 1.000 0.120 MT 15061 synonymous variant A/G snv 0.700 0
dbSNP: rs527236206
rs527236206
CYTB ; ND6
1 1.000 0.120 MT 15148 synonymous variant G/A snv 0.700 0
dbSNP: rs527236207
rs527236207
CYTB ; ND6
1 1.000 0.120 MT 15259 synonymous variant C/T snv 0.700 0