List of variants in gene STXBP1 reported as benign by Ambry Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_001032221.6(STXBP1):c.846C>T (p.Asp282=)	rs58889246	0.05156
NM_001032221.6(STXBP1):c.38-3T>C	rs138763389	0.01315
NM_001032221.6(STXBP1):c.1356C>T (p.Thr452=)	rs35099393	0.00894
NM_001032221.6(STXBP1):c.250G>A (p.Val84Ile)	rs34830702	0.00033
NM_001032221.6(STXBP1):c.1351G>A (p.Val451Ile)	rs150259704	0.00021
NM_001032221.6(STXBP1):c.1548-7_1548-4del	rs796053349

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