"Genetic Services Laboratory, University of Chicago"[submitter] AND "N - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 129765	NM_020999.4(NEUROG3):c.596T>C (p.Phe199Ser)	NEUROG3 (F199S)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 129764	NM_020999.4(NEUROG3):c.499G>A (p.Gly167Arg)	NEUROG3 (G167R)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign
Select item 435975	NM_020999.4(NEUROG3):c.162C>A (p.Cys54Ter)	NEUROG3 (C54*)	Single nucleotide variant (nonsense)	not provided +1 more	GConflicting classifications of pathogenicity

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