RS730882215 WWOX

Health Risk Chr 16:78424869
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What This Variant Does
"CLNSIG=4
Associated Conditions
Global developmental delay
Brain atrophy
Abnormal facial shape
Developmental and epileptic encephalopathy
28
Autosomal recessive spinocerebellar ataxia 12
1
WWOX-related disorder
Esophageal squamous cell carcinoma
Global developmental delay
Brain atrophy
Abnormal facial shape
Developmental and epileptic encephalopathy
28
Autosomal recessive spinocerebellar ataxia 12
Other Variants in WWOX
rs587777127 rs587777128 rs587777248 rs730880290 rs730880291 rs730880292 rs79771882 rs751181600 rs878855021 rs756762196
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