RS2065944203 MECP2

Health Risk Chr X:154031064
Upload your DNA to see your genotype for this variant.
Associated Conditions
Inborn genetic diseases
Severe neonatal-onset encephalopathy with microcephaly
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