List of variants in gene EIF2B2 reported as benign for Vanishing white matter disease

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_014239.4(EIF2B2):c.434-11C>T	rs200995477	0.00034
NM_014239.4(EIF2B2):c.899-11T>G	rs78900727	0.00034
NM_014239.4(EIF2B2):c.982A>G (p.Ile328Val)	rs145117455	0.00010

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