C0796222[trait identifier] AND "New York Genome Center"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 143710	NM_001110792.2(MECP2):c.872C>T (p.Ala291Val)	MECP2 (A279V +3 more)	Single nucleotide variant (missense variant)	Rett syndrome	GLikely pathogenicFDA Recognized database
Select item 156669	NM_001110792.2(MECP2):c.727G>A (p.Gly243Arg)	MECP2 (G231R +3 more)	Single nucleotide variant (missense variant)	Rett syndrome	GLikely benignFDA Recognized database