List of variants in gene LDLR reported as benign for multiple congenital anomalies/dysmorphic syndrome

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_000527.5(LDLR):c.81C>T (p.Cys27=)	rs2228671	0.08613
NM_000527.5(LDLR):c.1617C>T (p.Pro539=)	rs5929	0.07003

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