ClinVar Miner

List of variants in gene combination SCO2, TYMP reported as likely benign for Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency

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Total variants: 3
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HGVS dbSNP
NM_001169109.1(SCO2):c.-14+653_-14+656dup rs143413019
NM_001257988.1(TYMP):c.831G>A (p.Leu277=) rs8141558
NM_001953.4(TYMP):c.929-6_929-3del rs201685922

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