RS748262024 SETX

Health Risk Chr 9:132327510
Upload your DNA to see your genotype for this variant.
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
Ask Dr. Hemsworth about this variant