RS61748421 MECP2
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What This Variant Does
"MECP2 Rett syndrome mutation
Associated Conditions
Rett syndrome
Intellectual disability
Global developmental delay
Developmental regression
Severe neonatal-onset encephalopathy with microcephaly
Inborn genetic diseases
Syndromic X-linked intellectual disability Lubs type
MECP2-related disorder
Rett syndrome
Intellectual disability
Global developmental delay
Developmental regression
Severe neonatal-onset encephalopathy with microcephaly
Inborn genetic diseases
Syndromic X-linked intellectual disability Lubs type
Other Variants in MECP2