List of variants in gene EIF2B4 reported as likely pathogenic 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001034116.2(EIF2B4):c.32-1G>T	rs1682246203
NM_001034116.2(EIF2B4):c.414dup (p.Ser139fs)	rs1682104932
NM_001034116.2(EIF2B4):c.498+2_498+5del
NM_001034116.2(EIF2B4):c.551C>T (p.Pro184Leu)	rs1682025430

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