ClinVar Miner

List of variants in gene combination MT-ATP6, MT-ATP8 reported as uncertain significance for Leigh syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NC_012920.1:m.8540T>C	rs878852987
NC_012920.1:m.8550A>G	rs1603221581
NC_012920.1:m.8568C>A	rs1603221589

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