rs115532916
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs115532916
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs368949613
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs377022708
|
ACAD9;KIAA1257
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs377022708
|
ACAD9;KIAA1257
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
T |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs387907041
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs387907042
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
A |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs1057518752
|
ACAD9;KIAA1257
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
G |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs143383023
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs149753643
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs377547811
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs762521317
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
T |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs368949613
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.800 |
GeneticVariation |
UNIPROT |
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.
|
26741492 |
2016 |
rs387907041
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.800 |
GeneticVariation |
UNIPROT |
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.
|
26741492 |
2016 |
rs387907042
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.800 |
GeneticVariation |
UNIPROT |
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.
|
26741492 |
2016 |
rs139145143
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.700 |
GeneticVariation |
UNIPROT |
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.
|
26741492 |
2016 |
rs1447947184
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.700 |
GeneticVariation |
UNIPROT |
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.
|
26741492 |
2016 |
rs777282696
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.700 |
GeneticVariation |
UNIPROT |
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.
|
26741492 |
2016 |
rs781149699
|
ACAD9;KIAA1257
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.700 |
GeneticVariation |
UNIPROT |
A Comprehensive Genomic Analysis Reveals the Genetic Landscape of Mitochondrial Respiratory Chain Complex Deficiencies.
|
26741492 |
2016 |
rs368949613
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.800 |
GeneticVariation |
UNIPROT |
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency.
|
17564966 |
2007 |
rs387907041
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.800 |
GeneticVariation |
UNIPROT |
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency.
|
17564966 |
2007 |
rs387907042
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.800 |
GeneticVariation |
UNIPROT |
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency.
|
17564966 |
2007 |
rs139145143
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.700 |
GeneticVariation |
UNIPROT |
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency.
|
17564966 |
2007 |
rs1447947184
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.700 |
GeneticVariation |
UNIPROT |
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency.
|
17564966 |
2007 |
rs777282696
|
Entrez Id: |
28976 |
Gene Symbol: |
ACAD9 |
ACAD9
|
MITOCHONDRIAL COMPLEX I DEFICIENCY, NUCLEAR TYPE 20
|
|
0.700 |
GeneticVariation |
UNIPROT |
A new genetic disorder in mitochondrial fatty acid beta-oxidation: ACAD9 deficiency.
|
17564966 |
2007 |