RS117861188 SETX

Health Risk Chr 9:132336359 snv missense variant
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Associated Conditions
Amyotrophic lateral sclerosis type 4
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Hereditary spastic paraplegia
Inborn genetic diseases
SETX-related disorder
Amyotrophic lateral sclerosis type 4
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Hereditary spastic paraplegia
Inborn genetic diseases
SETX-related disorder
Population Frequencies
gnomAD ALL
0.1%
1kG AFR
100%
1kG ALL
100%
1kG AMR
100%
1kG EAS
100%
1kG EUR
99.8%
1kG SAS
100%
Other Variants in SETX
rs121434376 rs121434377 rs587776536 rs29001665 rs29001584 rs28941475 rs121434378 rs121434379 rs121434380 rs121434381
Ask Dr. Hemsworth about this variant