"PreventionGenetics, part of Exact Sciences"[submitter] AND "EIF2B1"[g - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 258089	NM_001414.4(EIF2B1):c.*49G>A	EIF2B1, LOC126861664	Single nucleotide variant (3 prime UTR variant)	Vanishing white matter disease +1 more	GBenign
Select item 2892296	NM_001414.4(EIF2B1):c.765C>T (p.Asp255=)	EIF2B1, LOC126861664	Single nucleotide variant (synonymous variant)	EIF2B1-related disorder +1 more	GLikely benign
Select item 258092	NM_001414.4(EIF2B1):c.551+38C>A	EIF2B1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 258091	NM_001414.4(EIF2B1):c.483-22G>T	EIF2B1	Single nucleotide variant (intron variant)	not specified	GBenign
Select item 93731	NM_001414.4(EIF2B1):c.370-20A>G	EIF2B1	Single nucleotide variant (intron variant)	not specified +1 more	GBenign
Select item 258090	NM_001414.4(EIF2B1):c.369+50C>T	EIF2B1	Single nucleotide variant (intron variant)	not specified	GLikely benign

ClinVar