"Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 95379	NM_006363.6(SEC23B):c.1233+9A>G	SEC23B	Single nucleotide variant (intron variant)	not provided +3 more	GBenign
Select item 167666	NM_006363.6(SEC23B):c.1276G>A (p.Val426Ile)	SEC23B (V426I +1 more)	Single nucleotide variant (missense variant)	Congenital dyserythropoietic anemia, type II +3 more	GBenign/Likely benign
Select item 95385	NM_006363.6(SEC23B):c.1744-20T>A	SEC23B	Single nucleotide variant (intron variant)	Congenital dyserythropoietic anemia, type II +3 more	GBenign

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