List of variants in gene MT-TT 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: 36

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.15889T>C	rs199833246
NC_012920.1(MT-CYB):m.15891C>T	rs1556424681
NC_012920.1(MT-CYB):m.15892T>C	rs1556424683
NC_012920.1(MT-CYB):m.15894G>A	rs1569484752
NC_012920.1(MT-CYB):m.15900T>C	rs878927456
NC_012920.1(MT-CYB):m.15902A>G	rs1556424685
NC_012920.1(MT-CYB):m.15903A>G	rs1603225580
NC_012920.1(MT-CYB):m.15904C>T	rs35788393
NC_012920.1(MT-CYB):m.15905T>C	rs879126276
NC_012920.1(MT-CYB):m.15907A>G	rs41383248
NC_012920.1(MT-CYB):m.15908T>C	rs386829266
NC_012920.1(MT-CYB):m.15913C>T	rs1603225584
NC_012920.1(MT-CYB):m.15914A>G	rs1603225587
NC_012920.1(MT-CYB):m.15916T>C	rs1603225591
NC_012920.1(MT-CYB):m.15924A>G	rs193303001
NC_012920.1(MT-CYB):m.15926C>T	rs1603225597
NC_012920.1(MT-CYB):m.15929A>G	rs878866272
NC_012920.1(MT-CYB):m.15930G>A	rs41441949
NC_012920.1(MT-CYB):m.15932T>C	rs527236199
NC_012920.1(MT-CYB):m.15935A>G	rs1556424699
NC_012920.1(MT-CYB):m.15936A>T	rs1556424701
NC_012920.1(MT-CYB):m.15937A>G	rs1603225605
NC_012920.1(MT-CYB):m.15938C>T	rs200572753
NC_012920.1(MT-CYB):m.15939C>T	rs878981265
NC_012920.1(MT-CYB):m.15940T>C	rs879197567
NC_012920.1(MT-CYB):m.15941T>C	rs193303003
NC_012920.1(MT-CYB):m.15942T>C	rs28535186
NC_012920.1(MT-CYB):m.15944del	rs1603225607
NC_012920.1(MT-CYB):m.15944dup	rs1603225607
NC_012920.1(MT-CYB):m.15946C>T	rs202014122
NC_012920.1(MT-CYB):m.15947A>G	rs1556424708
NC_012920.1(MT-CYB):m.15949G>A	rs1603225611
NC_012920.1(MT-CYB):m.15951A>G	rs199993959
NC_012920.1:m.15927G>A	rs193303002
NC_012920.1:m.15928G>A	rs527236198
NC_012920.1:m.15943T>C	rs527236200

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