List of variants in gene MT-TQ 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: 4

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HGVS	dbSNP
NC_012920.1(MT-CYB):m.4339G>A	rs1603219415
NC_012920.1(MT-CYB):m.4360G>A	rs1603219422
NC_012920.1(MT-CYB):m.4399T>C	rs1603219445
NC_012920.1(MT-CYB):m.4400A>G	rs1603219449

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