List of variants in gene MT-TN reported as uncertain significance for Juvenile myopathy, encephalopathy, lactic acidosis AND stroke

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: 5

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HGVS	dbSNP
NC_012920.1(MT-CYB):m.5661A>G	rs1603220076
NC_012920.1(MT-CYB):m.5669G>A	rs1603220083
NC_012920.1(MT-CYB):m.5672T>C	rs1603220085
NC_012920.1(MT-CYB):m.5693T>C	rs1603220092
NC_012920.1(MT-CYB):m.5708C>A	rs1603220094

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