C4225231[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1255586	NM_002336.3(LRP6):c.3406C>T (p.Arg1136Trp)	LRP6 (R1136W)	Single nucleotide variant (missense variant)	Tooth agenesis, selective, 7 +1 more	GUncertain significance
Select item 947760	NM_002336.3(LRP6):c.1243C>T (p.Arg415Ter)	LRP6 (R415*)	Single nucleotide variant (nonsense)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 620374	NM_002336.3(LRP6):c.1003C>T (p.Arg335Ter)	LRP6 (R335*)	Single nucleotide variant (nonsense)	Tooth agenesis, selective, 7 +2 more	GPathogenic/Likely pathogenic

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