ClinVar Miner

List of variants in gene SCO2 studied for Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency

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Total variants: 5
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NM_001169109.1(SCO2):c.-14+505G>A rs375309432
NM_001169109.1(SCO2):c.-14+646G>C rs145052206
NM_001169109.1(SCO2):c.-14+674G>C rs554814235
NM_001169109.1(SCO2):c.-14+705A>G rs886057632
NM_001169109.1(SCO2):c.-14+737C>T rs886057631

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