RS121909344 DCTN1

Health Risk Chr 2:74366896
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Amyotrophic lateral sclerosis
susceptibility to
Charcot-Marie-Tooth disease
Perry syndrome
Neuronopathy
distal hereditary motor
type 7B
Amyotrophic lateral sclerosis type 1
Inborn genetic diseases
DCTN1-related disorder
Amyotrophic lateral sclerosis
susceptibility to
Charcot-Marie-Tooth disease
Perry syndrome
Neuronopathy
Other Variants in DCTN1
rs121909342 rs121909343 rs72466485 rs72466487 rs67586389 rs17721059 rs886039228 rs886039227 rs576198476 rs886043620
Ask Dr. Hemsworth about this variant