C1854469[trait identifier] AND "Genetics and Molecular Pathology, SA P - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1006717	NM_006767.4(LZTR1):c.361C>T (p.His121Tyr)	LZTR1 (H121Y)	Single nucleotide variant (missense variant)	Noonan syndrome 10 +4 more	GUncertain significance
Select item 599030	NM_006767.4(LZTR1):c.628C>T (p.Arg210Ter)	LZTR1 (R210*)	Single nucleotide variant (nonsense)	LZTR1-related disorder +5 more	GPathogenic
Select item 546216	NM_006767.4(LZTR1):c.1785+1G>A	LZTR1	Single nucleotide variant (splice donor variant)	not provided +4 more	GPathogenic/Likely pathogenic

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