RS368928190 WWOX

Health Risk Chr 16:78425013
Upload your DNA to see your genotype for this variant.
What This Variant Does
"CLNSIG=5
Associated Conditions
Autosomal recessive spinocerebellar ataxia 12
Developmental and epileptic encephalopathy
1
Inborn genetic diseases
28
Autosomal recessive spinocerebellar ataxia 12
Developmental and epileptic encephalopathy
1
Inborn genetic diseases
28
Other Variants in WWOX
rs587777127 rs587777128 rs587777248 rs730880290 rs730880291 rs730880292 rs730882215 rs79771882 rs751181600 rs878855021
Ask Dr. Hemsworth about this variant