RS121434376 SETX

Health Risk Chr 9:132327511
Upload your DNA to see your genotype for this variant.
What This Variant Does
"[OMIM:?]
Associated Conditions
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Inborn genetic diseases
SETX-related disorder
Amyotrophic lateral sclerosis type 4
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Inborn genetic diseases
SETX-related disorder
Amyotrophic lateral sclerosis type 4
Other Variants in SETX
rs121434377 rs587776536 rs29001665 rs29001584 rs28941475 rs121434378 rs121434379 rs121434380 rs121434381 rs587776537
Ask Dr. Hemsworth about this variant