ClinVar Miner

List of variants in gene MECP2 reported as likely benign for Angelman syndrome; Mental retardation, X-linked, syndromic 13; Rett syndrome

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Total variants: 4
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HGVS dbSNP
NM_004992.3(MECP2):c.1154C>A (p.Pro385His) rs111302745
NM_004992.3(MECP2):c.420G>A (p.Ala140=) rs782082759
NM_004992.3(MECP2):c.450G>C (p.Leu150=) rs1060504124
NM_004992.3(MECP2):c.561C>A (p.Gly187=) rs200074866

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