ClinVar Miner

List of variants in gene combination COX15, ENTPD7 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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NM_020354.5(ENTPD7):c.*5070A>G rs73345141
NM_020354.5(ENTPD7):c.*5463T>G rs1056844
NM_020354.5(ENTPD7):c.*6487A>G rs10883407

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