List of variants in gene MT-TC reported as benign 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: 19

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HGVS	dbSNP
NC_012920.1(MT-CYB):m.5772G>A	rs1556423031
NC_012920.1(MT-CYB):m.5773G>A	rs9659239
NC_012920.1(MT-CYB):m.5774T>C	rs1603220102
NC_012920.1(MT-CYB):m.5774T>G	rs1603220102
NC_012920.1(MT-CYB):m.5775T>C	rs1603220105
NC_012920.1(MT-CYB):m.5780G>A	rs878999194
NC_012920.1(MT-CYB):m.5783G>A	rs1603220110
NC_012920.1(MT-CYB):m.5785T>C	rs373493739
NC_012920.1(MT-CYB):m.5786T>C	rs1603220117
NC_012920.1(MT-CYB):m.5788T>C	rs1556423033
NC_012920.1(MT-CYB):m.5794T>C	rs1556423035
NC_012920.1(MT-CYB):m.5806T>C	rs879211572
NC_012920.1(MT-CYB):m.5811A>G	rs1603220136
NC_012920.1(MT-CYB):m.5817C>T	rs1603220138
NC_012920.1(MT-CYB):m.5821G>A	rs56133209
NC_012920.1(MT-CYB):m.5822G>A	rs1556423041
NC_012920.1(MT-CYB):m.5823A>G	rs878875817
NC_012920.1(MT-CYB):m.5824G>A	rs879140945
m.5814T>C	rs200077222

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