List of variants in gene STXBP2 reported as likely benign by Genetic Services Laboratory, University of Chicago

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_006949.4(STXBP2):c.1298C>T (p.Ala433Val)	rs141309384	0.00866
NM_006949.4(STXBP2):c.1538+10C>T	rs139200597	0.00210
NM_006949.4(STXBP2):c.165C>T (p.Ile55=)	rs11538945	0.00103
NM_006949.4(STXBP2):c.1569G>A (p.Lys523=)	rs148868283	0.00054
NM_006949.4(STXBP2):c.497C>T (p.Thr166Met)	rs181216956	0.00031

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