List of variants in gene combination DNM1L, YARS2 reported as uncertain significance 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001040436.3(YARS2):c.126_127del	rs141873255	0.00126
NM_001040436.3(YARS2):c.*360A>G	rs567955032	0.00069
NM_001040436.3(YARS2):c.*142T>C	rs190589666	0.00010
NM_001040436.3(YARS2):c.*230A>G	rs371690622	0.00001
NM_001040436.3(YARS2):c.*62G>A	rs527443669

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