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: rs755933881
rs755933881
1 226982969 missense variant G/A snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 0
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: 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: 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: rs80356529
rs80356529
0.827 0.240 3 193643996 missense variant G/A;C snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs80356530
rs80356530
0.882 0.320 3 193667168 splice region variant TTAG/- delins
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs875989831
rs875989831
1.000 3 101565595 missense variant A/G snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs886041081
rs886041081
0.925 4 185144891 missense variant G/A snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 0
dbSNP: rs886041082
rs886041082
1.000 4 185145863 missense variant C/G snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 0
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: rs746538436
rs746538436
5 74746138 frameshift variant T/- del
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs761283105
rs761283105
5 74747731 missense variant C/T snv 1.6E-05 2.8E-05
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 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: rs144972972
rs144972972
1.000 6 151430154 missense variant T/C snv 2.0E-04 2.4E-04
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2016 2016
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: rs397515421
rs397515421
1.000 6 151405787 missense variant C/T snv 2.0E-05 2.1E-05
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2016 2016
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
dbSNP: rs773470671
rs773470671
6 151427481 splice donor variant C/T snv 2.4E-05
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs886037771
rs886037771
6 151405734 missense variant G/A snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs886037772
rs886037772
6 151436494 stop gained G/A snv 7.0E-06
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs886037773
rs886037773
6 151405719 splice donor variant C/A;G snv 4.0E-06
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2016 2016
dbSNP: rs515726180
rs515726180
8 102238827 splice region variant C/T snv 8.0E-06 2.1E-05
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: 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