List of variants in gene MT-TS2 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: 7

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.12213G>A	rs1603223616
NC_012920.1(MT-CYB):m.12218C>A	rs1603223621
NC_012920.1(MT-CYB):m.12230A>G	rs1603223625
NC_012920.1(MT-CYB):m.12241dup	rs1603223633
NC_012920.1(MT-CYB):m.12247T>C	rs1603223637
NC_012920.1(MT-CYB):m.12250C>T	rs1603223639
NC_012920.1(MT-CYB):m.12255T>C	rs1603223640

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