RS61752992 MECP2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rett syndrome
zappella variant
Severe neonatal-onset encephalopathy with microcephaly
Autism
susceptibility to
X-linked 3
X-linked intellectual disability-psychosis-macroorchidism syndrome
Delayed gross motor development
Loss of ambulation
Delayed speech and language development
Smith-Magenis Syndrome-like
Inborn genetic diseases
Syndromic X-linked intellectual disability Lubs type
See cases
MECP2-related disorder
Other Variants in MECP2