List of variants in gene SEC23B reported as uncertain significance for Congenital dyserythropoietic anemia

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_006363.5(SEC23B):c.-52T>G	rs191103191	0.00681
NM_006363.5(SEC23B):c.-76G>C	rs373348732	0.00050
NM_006363.5(SEC23B):c.-80G>A	rs886056524	0.00001
NM_006363.5(SEC23B):c.-94C>G	rs886056523

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