List of variants in gene SEC23B reported as uncertain significance by GeneDx

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_006363.6(SEC23B):c.1665+6T>C	rs371786580	0.00044
NM_006363.6(SEC23B):c.358G>A (p.Val120Met)	rs372784283	0.00029
NM_006363.6(SEC23B):c.1873C>A (p.Leu625Ile)	rs368458175	0.00001
NM_006363.6(SEC23B):c.890C>T (p.Thr297Ile)	rs1363436677	0.00001
NM_006363.6(SEC23B):c.256A>G (p.Asn86Asp)	rs761424294

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