ClinVar Miner

List of variants reported as uncertain significance for Rett syndrome by Integrated Genetics/Laboratory Corporation of America

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Total variants: 5
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HGVS dbSNP
NM_001110792.2(MECP2):c.1250C>T (p.Pro417Leu) rs61753016
NM_004992.3(MECP2):c.1441G>A (p.Val481Met) rs193922678
NM_004992.3(MECP2):c.678T>G (p.Phe226Leu) rs878853313
NM_004992.3(MECP2):c.898G>A (p.Val300Ile) rs61751370
NM_004992.3(MECP2):c.909C>G (p.Ile303Met) rs61751439

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