RS267608571 MECP2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
X-linked intellectual disability-psychosis-macroorchidism syndrome
Intellectual disability
Rett syndrome
Severe neonatal-onset encephalopathy with microcephaly
X-linked MECP2-related disorders
X-linked intellectual disability-psychosis-macroorchidism syndrome
Intellectual disability
Rett syndrome
Severe neonatal-onset encephalopathy with microcephaly
X-linked MECP2-related disorders
Other Variants in MECP2