C5436781[trait identifier] AND "Greenwood Genetic Center Diagnostic La - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 422103	NM_001303256.3(MORC2):c.394C>T (p.Arg132Cys)	MORC2 (R132C +1 more)	Single nucleotide variant (missense variant)	Neurodevelopmental disorder +6 more	GConflicting classifications of pathogenicity
Select item 992297	NM_001303256.3(MORC2):c.328C>T (p.Arg110Cys)	MORC2 (R110C +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity