RS104894619 PMP22
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Hereditary liability to pressure palsies
Charcot-Marie-Tooth disease
type 1a
autosomal recessive
type IA
type I
Tip-toe gait
Charcot-Marie-Tooth disease type 1E
6 conditions
Hereditary liability to pressure palsies
Charcot-Marie-Tooth disease
type 1a
autosomal recessive
type IA
type I
Other Variants in PMP22