RS267608463 MECP2

Health Risk Chr X:154032206
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Rett syndrome
Rett syndrome
Bruxism
Delayed speech and language development
Stereotypic movement disorder
Delayed gross motor development
Rett syndrome
Rett syndrome
Bruxism
Delayed speech and language development
Stereotypic movement disorder
Delayed gross motor development
Other Variants in MECP2
rs28934904 rs28934905 rs28934906 rs28934907 rs61750240 rs63094662 rs267608434 rs61751362 rs28934908 rs28935468
Ask Dr. Hemsworth about this variant