ClinVar Miner

List of variants in gene SEC23B reported as likely benign for Congenital dyserythropoietic anemia

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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)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006363.5(SEC23B):c.-57G>C	rs113396443	0.01206
NM_006363.6(SEC23B):c.9_10del	rs142180765

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