Variant | Gene | Risk Allele | Score vda | Association Type | Original DB | Sentence supporting the association | PMID | PMID Year | ||
---|---|---|---|---|---|---|---|---|---|---|
|
0.800 | GeneticVariation | UNIPROT | High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. | 20818383 | 2010 |
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|
0.800 | GeneticVariation | UNIPROT | High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. | 20818383 | 2010 |
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|
0.800 | GeneticVariation | UNIPROT | High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency. | 20818383 | 2010 |
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|
0.800 | GeneticVariation | UNIPROT | De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency. | 14705112 | 2004 |
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|
0.800 | GeneticVariation | UNIPROT | De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency. | 14705112 | 2004 |
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|
0.800 | GeneticVariation | UNIPROT | De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency. | 14705112 | 2004 |
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|
0.800 | GeneticVariation | UNIPROT | Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene. | 11456298 | 2001 |
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|
0.800 | GeneticVariation | UNIPROT | Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene. | 11456298 | 2001 |
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|
0.800 | GeneticVariation | UNIPROT | Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene. | 11456298 | 2001 |