ClinVar Miner

List of variants in gene MECP2 reported as pathogenic for Severe neonatal-onset encephalopathy with microcephaly; MECP2 duplication syndrome; Mental retardation, X-linked, syndromic 13; Rett syndrome

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Total variants: 1
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NM_004992.3(MECP2):c.1101_1201del (p.His367fs) rs1557135315

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