RS111537259 SETX

Health Risk Chr 9:132328417
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Associated Conditions
Inborn genetic diseases
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Amyotrophic lateral sclerosis type 4
Inborn genetic diseases
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Amyotrophic lateral sclerosis type 4
Other Variants in SETX
rs121434376 rs121434377 rs587776536 rs29001665 rs29001584 rs28941475 rs121434378 rs121434379 rs121434380 rs121434381
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