List of variants in gene LRP6 reported as benign for cardiovascular disorder

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_002336.3(LRP6):c.2382C>T (p.Asn794=)	rs74774620	0.00556
NM_002336.3(LRP6):c.3192A>G (p.Val1064=)	rs114714311	0.00552

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