RS886056332 DCTN1

Health Risk Chr 2:74370333
Upload your DNA to see your genotype for this variant.
Associated Conditions
Perry syndrome
Neuronopathy
distal hereditary motor
type 7B
Inborn genetic diseases
Amyotrophic lateral sclerosis type 1
DCTN1-related disorder
Perry syndrome
Neuronopathy
distal hereditary motor
type 7B
Inborn genetic diseases
Amyotrophic lateral sclerosis type 1
DCTN1-related disorder
Other Variants in DCTN1
rs121909342 rs121909343 rs121909344 rs72466485 rs72466487 rs67586389 rs17721059 rs886039228 rs886039227 rs576198476
Ask Dr. Hemsworth about this variant