List of variants in gene MECP2 reported as uncertain significance by Department of Genetics, Rouen University Hospital, Normandy Center for Genomic and Personalized Medicine

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.1084_1314del (p.Ser362_Ser438del)	rs2148659063
NM_001110792.2(MECP2):c.556A>C (p.Lys186Gln)	rs781912934
NM_001110792.2(MECP2):c.60A>C (p.Arg20Ser)	rs2522549346

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