List of variants in gene MT-TT 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: 6

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HGVS	dbSNP
NC_012920.1(MT-CYB):m.15888G>A	rs1603225568
NC_012920.1(MT-CYB):m.15890C>T	rs527236196
NC_012920.1(MT-CYB):m.15897G>A	rs1603225575
NC_012920.1(MT-CYB):m.15909A>T	rs1556424690
NC_012920.1(MT-CYB):m.15921T>C	rs1603225593
m.15950G>A	rs118203890

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