RS145097270 SETX
Upload your DNA to see your genotype for this variant.
Associated Conditions
Hereditary spastic paraplegia
Amyotrophic lateral sclerosis type 4
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Inborn genetic diseases
Amyotrophic lateral sclerosis
SETX-related disorder
Hereditary spastic paraplegia
Amyotrophic lateral sclerosis type 4
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Inborn genetic diseases
Amyotrophic lateral sclerosis
Other Variants in SETX