RS104894622 PMP22

Health Risk Chr 17:15260692
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
DEJERINE-SOTTAS SYNDROME
AUTOSOMAL DOMINANT
Charcot-Marie-Tooth disease
type I
Inborn genetic diseases
Dejerine-Sottas disease
Roussy-Lévy syndrome
Charcot-Marie-Tooth disease
type I
DEJERINE-SOTTAS SYNDROME
AUTOSOMAL DOMINANT
Charcot-Marie-Tooth disease
type I
Inborn genetic diseases
Dejerine-Sottas disease
Other Variants in PMP22
rs104894617 rs104894618 rs104894619 rs104894620 rs104894621 rs587776691 rs104894623 rs80338763 rs786205087 rs104894624
Ask Dr. Hemsworth about this variant