List of variants in gene MT-TW 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: 7

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HGVS	dbSNP	gnomAD frequency
NC_012920.1(MT-TW):m.5521G>A	rs199474673
NC_012920.1(MT-TW):m.5532G>A	rs199474674
NC_012920.1(MT-TW):m.5536_5537insT	rs1603220010
NC_012920.1(MT-TW):m.5538G>A	rs1603220012
NC_012920.1(MT-TW):m.5540G>A	rs1603220014
NC_012920.1(MT-TW):m.5543T>C	rs1603220016
m.5556G>A	rs387906736

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