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No pathogenic/probable pathogenic variants that are highly correlated with the clinical phenotype of the subject were found on the mitochondrial genome.
| Gene | Genome location | dbSNP ID | Variation naming | Variation type | Variation abundance | Variation classification | Relative monitoring results | |
|---|---|---|---|---|---|---|---|---|
| Father | Mother | |||||||
| / | / | / | / | / | / | / | / | / |
