RS61750256 MECP2

Health Risk Chr X:154030969
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rett syndrome
Severe neonatal-onset encephalopathy with microcephaly
Inborn genetic diseases
Rett syndrome
Severe neonatal-onset encephalopathy with microcephaly
Inborn genetic diseases
Other Variants in MECP2
rs28934904 rs28934905 rs28934906 rs28934907 rs61750240 rs63094662 rs267608434 rs61751362 rs28934908 rs28935468
Ask Dr. Hemsworth about this variant