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: 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: 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: 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: 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: rs1554887222
rs1554887222
10 100989791 missense variant T/C snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
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: rs370475970
rs370475970
16 1985996 missense variant C/T snv 3.2E-05 7.7E-05
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: rs376902371
rs376902371
1.000 17 18308367 missense variant T/C snv 6.4E-05 3.5E-05
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2018 2018
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: 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: 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: 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: 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: rs772751581
rs772751581
14 22769791 missense variant G/T snv 4.0E-06
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2018 2018
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: rs775256289
rs775256289
12 32750046 inframe insertion -/TGATCAGACATGACCTCC delins 1.6E-05
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs863224028
rs863224028
16 1984415 frameshift variant C/- 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