List of variants in gene HSPG2 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_005529.7(HSPG2):c.10702G>A (p.Val3568Ile)	rs115616224	0.00899
NM_005529.7(HSPG2):c.9719C>T (p.Ala3240Val)	rs62642505	0.00677
NM_005529.7(HSPG2):c.12004C>G (p.Leu4002Val)	rs140403186	0.00485

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