ClinVar Miner

List of variants in gene MT-CO2 studied for Hepatic failure, early-onset, and neurologic disorder due to cytochrome C oxidase deficiency

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Total variants: 6
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HGVS dbSNP
NC_012920.1:m.7965T>C rs1556423369
NC_012920.1:m.8088delT rs1556423388
m.7587T>C rs199474825
m.7671T>A rs199474827
m.7896G>A rs199474829
m.8042_8043delAT rs199474828

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