RS574962577 CCDC88C
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Associated Conditions
Inborn genetic diseases
Spinocerebellar ataxia type 40
Hydrocephalus
nonsyndromic
autosomal recessive 1
Inborn genetic diseases
Spinocerebellar ataxia type 40
Hydrocephalus
nonsyndromic
autosomal recessive 1
Other Variants in CCDC88C