List of variants in gene SH3PXD2B reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001017995.3(SH3PXD2B):c.1062+15G>A	rs111572530	0.01650
NM_001017995.3(SH3PXD2B):c.2477C>T (p.Pro826Leu)	rs73317796	0.01063
NM_001017995.3(SH3PXD2B):c.1612GAGCGG[2] (p.538ER[2])	rs534091900

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