Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1556424691
rs1556424691
CYTB ; ND6 ; TRNT
0.851 0.200 MT 15923 non coding transcript exon variant A/G snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 4 1993 2018
dbSNP: rs199474657
rs199474657
ND1 ; ND2 ; TRNL1
0.752 0.360 MT 3243 non coding transcript exon variant A/G snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 2 2001 2004
dbSNP: rs111033573
rs111033573
1.000 0.200 10 100989285 missense variant G/A;T snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs111033577
rs111033577
1.000 0.200 10 100989352 missense variant T/C;G snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs113994099
rs113994099
0.827 0.240 15 89320883 missense variant T/C snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.710 1.000 1 2007 2017
dbSNP: rs115079861
rs115079861
1.000 6 151405236 stop lost C/G;T snv 2.0E-05; 4.0E-03
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs121918054
rs121918054
0.807 0.240 15 89323460 missense variant C/G;T snv 6.9E-04; 4.0E-06
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs1365700579
rs1365700579
12 32750105 missense variant C/G;T snv 8.0E-06
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs1553877864
rs1553877864
3 193643430 missense variant C/T snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs1554042187
rs1554042187
5 74758878 missense variant T/G snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs1554887028
rs1554887028
10 100989213 missense variant C/A snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs1554887097
rs1554887097
0.807 0.320 10 100989331 missense variant G/A snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs1554887213
rs1554887213
1.000 0.200 10 100989774 splice acceptor variant G/T snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs1554887222
rs1554887222
10 100989791 missense variant T/C snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs1555745989
rs1555745989
0.925 0.040 19 1244118 missense variant T/G snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.710 1.000 1 2018 2018
dbSNP: rs1566433812
rs1566433812
14 22768050 frameshift variant -/CAGAGCAG delins
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2018 2018
dbSNP: rs199730889
rs199730889
1.000 3 101565323 missense variant G/A;T snv 4.0E-06; 1.1E-04
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs200944917
rs200944917
17 18305208 stop gained G/A;T snv 1.0E-04
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2018 2018
dbSNP: rs28937887
rs28937887
1.000 10 100989211 missense variant G/A;T snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs370863743
rs370863743
6 151436526 missense variant G/A;T snv 2.4E-05
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs387906899
rs387906899
1.000 3 193643609 missense variant A/G snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs398124298
rs398124298
0.925 0.160 3 193647110 missense variant C/A;G snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs515726199
rs515726199
1.000 0.200 8 102208239 frameshift variant A/- delins
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs746538436
rs746538436
5 74746138 frameshift variant T/- del
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs771894262
rs771894262
6 151433213 missense variant C/G;T snv 4.0E-06; 4.0E-06
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2016 2016