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

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_006363.6(SEC23B):c.1276G>A (p.Val426Ile)	rs41309927	0.04225
NM_006363.6(SEC23B):c.835-7A>G	rs184484121	0.00317
NM_006363.6(SEC23B):c.1512T>C (p.Asn504=)	rs138198461	0.00271
NM_006363.6(SEC23B):c.*278T>C	rs564007974	0.00004
NM_006363.6(SEC23B):c.773A>G (p.Gln258Arg)	rs534770840	0.00001

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