List of variants in gene MECP2 reported as likely pathogenic by Molecular Diagnostics Lab, Nemours Children's Health, Delaware

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_001110792.2(MECP2):c.1130_1174del (p.Glu377_Pro391del)	rs1064792899
NM_001110792.2(MECP2):c.352C>T (p.Arg118Trp)	rs28934907
NM_001110792.2(MECP2):c.437C>G (p.Ser146Cys)	rs61748390
NM_001110792.2(MECP2):c.504C>A (p.Asp168Glu)	rs61748408
NM_001110792.2(MECP2):c.509C>T (p.Thr170Met)	rs28934906
NM_001110792.2(MECP2):c.941C>T (p.Pro314Leu)	rs61749723
NM_001110792.2(MECP2):c.953G>A (p.Arg318His)	rs61751443

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