List of variants in gene EEF2 reported as benign for hereditary dementia

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_001961.4(EEF2):c.1632T>C (p.His544=)	rs36526	0.86134
NM_001961.4(EEF2):c.1150+15T>C	rs36525	0.86128

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