List of variants in gene MT-TK 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: 10

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.8308A>G	rs879081228
NC_012920.1(MT-CYB):m.8311T>C	rs371589230
NC_012920.1(MT-CYB):m.8337T>C	rs1603221405
NC_012920.1(MT-CYB):m.8343A>G	rs1603221411
NC_012920.1(MT-CYB):m.8345C>T	rs1603221413
NC_012920.1(MT-CYB):m.8347A>G	rs1603221417
NC_012920.1(MT-CYB):m.8348A>G	rs1556423430
NC_012920.1(MT-CYB):m.8349C>T	rs1603221418
NC_012920.1(MT-CYB):m.8360A>G	rs1603221422
m.8296A>G	rs118192102

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