RS61754425 MECP2

Health Risk Chr X:154032529
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What This Variant Does
"CLNSIG=5
Associated Conditions
Rett syndrome
Inborn genetic diseases
Rett syndrome
Inborn genetic diseases
Other Variants in MECP2
rs28934904 rs28934905 rs28934906 rs28934907 rs61750240 rs63094662 rs267608434 rs61751362 rs28934908 rs28935468
Ask Dr. Hemsworth about this variant