RS534886444 SETX
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Associated Conditions
Charcot-Marie-Tooth disease
Amyotrophic lateral sclerosis type 4
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Inborn genetic diseases
Charcot-Marie-Tooth disease
Amyotrophic lateral sclerosis type 4
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Inborn genetic diseases
Other Variants in SETX