List of variants in gene STXBP2 reported as uncertain significance for hematologic disorder

Minimum submission review status:		Collection method:
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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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006949.4(STXBP2):c.911C>T (p.Thr304Met)	rs200135215	0.00008
NM_006949.4(STXBP2):c.499C>T (p.Arg167Trp)	rs768296460	0.00006
NM_006949.4(STXBP2):c.1586G>C (p.Arg529Pro)	rs35490401

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