RS28936682 PMP22
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:DEJERINE-SOTTAS SYNDROME, AUTOSOMAL RECESSIVE]
Associated Conditions
Autosomal recessive Dejerine-Sottas syndrome
Charcot-Marie-Tooth disease type 1E
Charcot-Marie-Tooth disease
type I
Hereditary liability to pressure palsies
Autosomal recessive Dejerine-Sottas syndrome
Charcot-Marie-Tooth disease type 1E
Charcot-Marie-Tooth disease
type I
Hereditary liability to pressure palsies
Other Variants in PMP22