List of variants in gene MECP2 reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.1225G>A (p.Glu409Lys)	rs56268439	0.00308
NM_001110792.2(MECP2):c.626C>T (p.Thr209Met)	rs61749714	0.00064
NM_001110792.2(MECP2):c.1196C>T (p.Pro399Leu)	rs63390262	0.00010
NM_001110792.2(MECP2):c.414-17del	rs61753982

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