RS61748420 MECP2

Health Risk Chr X:154031329
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What This Variant Does
"CLNSIG=5
Associated Conditions
X-linked intellectual disability-psychosis-macroorchidism syndrome
Rett syndrome
Severe neonatal-onset encephalopathy with microcephaly
See cases
Inborn genetic diseases
MECP2-related disorder
X-linked intellectual disability-psychosis-macroorchidism syndrome
Rett syndrome
Severe neonatal-onset encephalopathy with microcephaly
See cases
Inborn genetic diseases
MECP2-related disorder
Other Variants in MECP2
rs28934904 rs28934905 rs28934906 rs28934907 rs61750240 rs63094662 rs267608434 rs61751362 rs28934908 rs28935468
Ask Dr. Hemsworth about this variant