List of variants in gene MT-TK 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.8301A>G	rs1603221396
NC_012920.1(MT-CYB):m.8311T>A	rs371589230
NC_012920.1(MT-CYB):m.8340_8341insT	rs1603221409
NC_012920.1(MT-CYB):m.8358A>G	rs1603221421
NC_012920.1(MT-CYB):m.8364A>T	rs1603221428

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