RS61749721 MECP2
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What This Variant Does
"MECP2 Rett syndrome mutation
Associated Conditions
Rett syndrome
X-linked intellectual disability-psychosis-macroorchidism syndrome
Severe neonatal-onset encephalopathy with microcephaly
Autism
susceptibility to
X-linked 3
Syndromic X-linked intellectual disability Lubs type
Abnormality of the nervous system
Inborn genetic diseases
Neurodevelopmental delay
MECP2-related disorder
Intellectual disability
Rett syndrome
X-linked intellectual disability-psychosis-macroorchidism syndrome
Severe neonatal-onset encephalopathy with microcephaly
Other Variants in MECP2