RS587776537 SETX

Health Risk Chr 9:132346304
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What This Variant Does
"CLNSIG=5
Associated Conditions
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Inborn genetic diseases
Spinocerebellar ataxia
autosomal recessive
with axonal neuropathy 2
Inborn genetic diseases
Other Variants in SETX
rs121434376 rs121434377 rs587776536 rs29001665 rs29001584 rs28941475 rs121434378 rs121434379 rs121434380 rs121434381
Ask Dr. Hemsworth about this variant