RS587783092 MECP2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Severe neonatal-onset encephalopathy with microcephaly
Severe neonatal-onset encephalopathy with microcephaly
Seizure
X-linked intellectual disability-psychosis-macroorchidism syndrome
Inborn genetic diseases
Severe neonatal-onset encephalopathy with microcephaly
Severe neonatal-onset encephalopathy with microcephaly
Seizure
X-linked intellectual disability-psychosis-macroorchidism syndrome
Inborn genetic diseases
Other Variants in MECP2