RS104894627 PMP22
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Charcot-Marie-Tooth disease
type 1a
with focally folded myelin sheaths
Charcot-Marie-Tooth disease
type 1a
with focally folded myelin sheaths
Other Variants in PMP22