"EIF2B3-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 716801	NM_020365.5(EIF2B3):c.983A>G (p.Lys328Arg)	EIF2B3 (K328R)	Single nucleotide variant (missense variant)	EIF2B3-related condition +2 more	GConflicting classifications of pathogenicity
Select item 874279	NM_020365.5(EIF2B3):c.785-6C>G	EIF2B3	Single nucleotide variant (intron variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 297445	NM_020365.5(EIF2B3):c.591G>A (p.Thr197=)	EIF2B3	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 4439	NM_020365.5(EIF2B3):c.260C>T (p.Ala87Val)	EIF2B3 (A87V)	Single nucleotide variant (missense variant)	EIF2B3-related condition +2 more	GConflicting classifications of pathogenicity
Select item 500850	NM_020365.5(EIF2B3):c.224T>C (p.Ile75Thr)	EIF2B3 (I75T)	Single nucleotide variant (missense variant)	EIF2B3-related condition +3 more	GLikely benign
Select item 95946	NM_020365.5(EIF2B3):c.149-4A>G	EIF2B3	Single nucleotide variant (intron variant)	EIF2B3-related condition +3 more	GBenign
Select item 2191024	NM_020365.5(EIF2B3):c.148+3G>A	EIF2B3	Single nucleotide variant (intron variant)	EIF2B3-related condition +1 more	GConflicting classifications of pathogenicity

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