RS202176679 MPZ

Health Risk Chr 1:161306116
Upload your DNA to see your genotype for this variant.
Associated Conditions
Charcot-Marie-Tooth disease dominant intermediate D
Roussy-Lévy syndrome
Charcot-Marie-Tooth disease
type I
Neuropathy
congenital hypomyelinating
2
Charcot-Marie-Tooth disease type 1B
Inborn genetic diseases
Charcot-Marie-Tooth disease dominant intermediate D
Roussy-Lévy syndrome
Charcot-Marie-Tooth disease
type I
Neuropathy
congenital hypomyelinating
Other Variants in MPZ
rs121913583 rs121913584 rs121913585 rs121913586 rs2102257349 rs121913587 rs121913588 rs121913589 rs121913590 rs121913593
Ask Dr. Hemsworth about this variant