List of variants in gene APOB reported as 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_000384.3(APOB):c.9880T>C (p.Ser3294Pro)	rs12720855	0.01525
NM_000384.3(APOB):c.7367C>A (p.Ala2456Asp)	rs12713675	0.01524
NM_000384.3(APOB):c.12697T>A (p.Ser4233Thr)	rs61743299	0.01522

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