List of variants in gene MECP2 reported as pathogenic by Laboratoire de Génétique Moléculaire, CHU Bordeaux

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.538C>T (p.Arg180Ter)	rs61748421
NM_001110792.2(MECP2):c.932_936delinsGCCCGAGAG (p.Thr311fs)
NM_001110792.2(MECP2):c.961C>T (p.Arg321Trp)	rs61751444

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