RS61748391 MECP2

Health Risk Chr X:154031425
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Rett syndrome
Inborn genetic diseases
Severe neonatal-onset encephalopathy with microcephaly
Rett syndrome
Inborn genetic diseases
Severe neonatal-onset encephalopathy with microcephaly
Other Variants in MECP2
rs28934904 rs28934905 rs28934906 rs28934907 rs61750240 rs63094662 rs267608434 rs61751362 rs28934908 rs28935468
Ask Dr. Hemsworth about this variant