List of variants in gene MT-TW 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: 8

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.5524T>C	rs1603220004
NC_012920.1(MT-CYB):m.5542C>T	rs1603220015
NC_012920.1(MT-CYB):m.5544T>C	rs1603220018
NC_012920.1(MT-CYB):m.5550C>T	rs1603220019
NC_012920.1(MT-CYB):m.5560G>A	rs1603220026
NC_012920.1(MT-CYB):m.5573A>G	rs1603220033
NC_012920.1(MT-CYB):m.5575T>C	rs1603220034
NC_012920.1:m.5559A>G	rs1556423008

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