C1970440[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 723536	NM_002336.3(LRP6):c.3192A>G (p.Val1064=)	LRP6	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 723537	NM_002336.3(LRP6):c.2382C>T (p.Asn794=)	LRP6	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign
Select item 689556	NM_002336.3(LRP6):c.2218C>T (p.Gln740Ter)	LRP6 (Q740*)	Single nucleotide variant (nonsense)	Tooth agenesis, selective, 7 +1 more	GPathogenic

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