List of variants in gene MT-TF 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: 15

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.592C>T	rs1603218450
NC_012920.1(MT-CYB):m.593T>C	rs879123694
NC_012920.1(MT-CYB):m.595dup	rs1603218451
NC_012920.1(MT-CYB):m.596T>C	rs1556422474
NC_012920.1(MT-CYB):m.597C>T	rs1603218453
NC_012920.1(MT-CYB):m.606A>G	rs200056066
NC_012920.1(MT-CYB):m.619T>C	rs1603218462
NC_012920.1(MT-CYB):m.629T>C	rs201031012
NC_012920.1(MT-CYB):m.630C>T	rs1603218468
NC_012920.1(MT-CYB):m.633A>G	rs1603218469
NC_012920.1(MT-CYB):m.634T>A	rs1603218470
NC_012920.1(MT-CYB):m.634T>C	rs1603218470
NC_012920.1(MT-CYB):m.635C>T	rs1603218471
NC_012920.1(MT-CYB):m.644A>G	rs1556422475
NC_012920.1(MT-CYB):m.647A>G	rs1569483788

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