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: rs1023075742
rs1023075742
1.000 22 42090742 start lost C/T snv 4.0E-06 2.1E-05
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 0
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: rs1131691575
rs1131691575
0.925 0.080 15 89317469 missense variant C/T snv 8.0E-06 1.4E-05
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs1131692061
rs1131692061
ND4 ; ND5 ; TRNL2
MT 12271 non coding transcript exon variant T/C snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 0
dbSNP: rs1131692062
rs1131692062
ND4 ; ND5 ; TRNL2
MT 12283 non coding transcript exon variant G/A snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 0
dbSNP: rs1131692063
rs1131692063
CYTB ; ND5
1.000 0.160 MT 13051 missense variant G/A snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 0
dbSNP: rs1131692064
rs1131692064
ATP6 ; ATP8 ; COX2 ; COX3
MT 7989 missense variant T/C snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 0
dbSNP: rs113994095
rs113994095
0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs113994096
rs113994096
0.827 0.080 15 89325639 missense variant G/A snv 1.5E-03 1.6E-03
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 1.000 1 2017 2017
dbSNP: rs113994097
rs113994097
0.724 0.400 15 89323426 missense variant C/G snv 9.7E-04 7.9E-04
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.720 1.000 1 2006 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: rs118192098
rs118192098
ATP6 ; ATP8 ; COX2 ; COX3 ; ND3 ; TRNK
0.851 0.200 MT 8344 non coding transcript exon variant A/G snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 0
dbSNP: rs121434453
rs121434453
CYTB ; ND6 ; TRNE
0.882 0.320 MT 14709 non coding transcript exon variant T/C snv
CUI: C0751651
Disease: Mitochondrial Diseases
Mitochondrial Diseases
0.700 0
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: 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: 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