List of variants in gene MT-TM 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: 6

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.4418T>C	rs1556422856
NC_012920.1(MT-CYB):m.4435A>G	rs878930498
NC_012920.1(MT-CYB):m.4452T>C	rs377043134
NC_012920.1(MT-CYB):m.4454T>A	rs11510098
NC_012920.1(MT-CYB):m.4454T>C	rs11510098
NC_012920.1(MT-CYB):m.4464G>A	rs1603219466

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