RS373375060 SETX

Health Risk Chr 9:132327373
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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
SETX-related disorder
Charcot-Marie-Tooth disease
Amyotrophic lateral sclerosis type 4
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Inborn genetic diseases
SETX-related disorder
Other Variants in SETX
rs121434376 rs121434377 rs587776536 rs29001665 rs29001584 rs28941475 rs121434378 rs121434379 rs121434380 rs121434381
Ask Dr. Hemsworth about this variant