List of variants in gene SEC23B reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_006363.6(SEC23B):c.1595G>C (p.Gly532Ala)	rs143456757	0.00207
NM_006363.6(SEC23B):c.993+10C>G	rs201948587	0.00173
NM_006363.6(SEC23B):c.66C>T (p.Asn22=)	rs144542988	0.00098
NM_006363.6(SEC23B):c.1198T>C (p.Phe400Leu)	rs142461689	0.00084
NM_006363.6(SEC23B):c.222-78C>T	rs150393520	0.00026
NM_006363.6(SEC23B):c.1884C>T (p.Tyr628=)	rs766473215	0.00007
NM_006363.6(SEC23B):c.1491C>T (p.Arg497=)	rs778443189	0.00004
NM_006363.6(SEC23B):c.1512-10G>T	rs770601333	0.00002
NM_006363.6(SEC23B):c.773A>G (p.Gln258Arg)	rs534770840	0.00001
NM_006363.6(SEC23B):c.1287T>C (p.Asn429=)
NM_006363.6(SEC23B):c.1816A>C (p.Arg606=)
NM_006363.6(SEC23B):c.2149-21TTG[6]
NM_006363.6(SEC23B):c.222-84A>G

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