C3810283[trait identifier] AND "St. Jude Molecular Pathology, St. Jude - ClinVar - NCBI

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1496147	NM_006767.4(LZTR1):c.22G>C (p.Gly8Arg)	LOC130067016, LZTR1 (G8R)	Single nucleotide variant (missense variant)	Schwannomatosis 2 +4 more	GUncertain significance
Select item 522164	NM_006767.4(LZTR1):c.26G>C (p.Gly9Ala)	LOC130067016, LZTR1 (G9A)	Single nucleotide variant (missense variant)	not specified +5 more	GConflicting classifications of pathogenicity
Select item 1098836	NM_006767.4(LZTR1):c.946G>A (p.Val316Met)	LZTR1 (V316M)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GUncertain significance
Select item 1020726	NM_006767.4(LZTR1):c.988A>G (p.Ser330Gly)	LZTR1 (S330G)	Single nucleotide variant (missense variant)	not provided +4 more	GUncertain significance
Select item 1098770	NM_006767.4(LZTR1):c.1412G>A (p.Arg471His)	LZTR1 (R471H)	Single nucleotide variant (missense variant)	Hereditary cancer-predisposing syndrome +5 more	GConflicting classifications of pathogenicity
Select item 968299	NM_006767.4(LZTR1):c.1700G>A (p.Arg567His)	LZTR1 (R567H)	Single nucleotide variant (missense variant)	Schwannomatosis 2 +5 more	GConflicting classifications of pathogenicity
Select item 1052307	NM_006767.4(LZTR1):c.2089C>T (p.Arg697Trp)	LZTR1 (R697W)	Single nucleotide variant (missense variant)	Noonan syndrome 10 +4 more	GUncertain significance
Select item 928713	NM_006767.4(LZTR1):c.2263C>T (p.Arg755Trp)	LZTR1 (R755W)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GUncertain significance