List of variants in gene MT-TF reported as pathogenic for hereditary skeletal muscle disorder

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: 4

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-CYB):m.583G>A	rs118203885
NC_012920.1(MT-CYB):m.586G>A	rs387906734
NC_012920.1(MT-CYB):m.611G>A	rs118203886
NC_012920.1(MT-CYB):m.616T>C	rs387906420

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