RS121913590 MPZ

Health Risk Chr 1:161306864
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What This Variant Does
"[OMIM:?]
Associated Conditions
Charcot-Marie-Tooth disease type 1B
Charcot-Marie-Tooth disease
type I
Neuropathy
congenital hypomyelinating
2
Autosomal dominant MPZ-related disorders
Charcot-Marie-Tooth disease type 1B
Charcot-Marie-Tooth disease
type I
Neuropathy
congenital hypomyelinating
2
Autosomal dominant MPZ-related disorders
Other Variants in MPZ
rs121913583 rs121913584 rs121913585 rs121913586 rs2102257349 rs121913587 rs121913588 rs121913589 rs121913593 rs121913594
Ask Dr. Hemsworth about this variant