List of variants in gene MECP2 reported as uncertain significance for History of neurodevelopmental disorder

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.1193_1198del (p.Leu398_Pro399del)	rs1569548334
NM_001110792.2(MECP2):c.379C>T (p.Arg127Cys)	rs267608388
NM_001110792.2(MECP2):c.785G>A (p.Arg262His)	rs61750227

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