List of variants in gene SLC16A1 reported as benign 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_003051.4(SLC16A1):c.1470T>A (p.Asp490Glu)	rs1049434	0.66103
NM_003051.4(SLC16A1):c.362-21A>C	rs201021807	0.26702

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