RS267607044 SETX
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Charcot-Marie-Tooth disease
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Amyotrophic lateral sclerosis type 4
Charcot-Marie-Tooth disease
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Amyotrophic lateral sclerosis type 4
Other Variants in SETX