RS572772837 SETX
Upload your DNA to see your genotype for this variant.
Associated Conditions
Amyotrophic lateral sclerosis type 4
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Inborn genetic diseases
SETX-related disorder
Cone-rod dystrophy
Amyotrophic lateral sclerosis type 4
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Inborn genetic diseases
Amyotrophic lateral sclerosis type 4
Spinocerebellar ataxia
autosomal recessive
Other Variants in SETX