RS56144125 TPP1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Neuronal ceroid lipofuscinosis 2
Autosomal recessive spinocerebellar ataxia 7
Inborn genetic diseases
Neuronal ceroid lipofuscinosis
TPP1-related disorder
Familial cancer of breast
Malignant tumor of urinary bladder
Ovarian serous cystadenocarcinoma
Lung cancer
Neuronal ceroid lipofuscinosis
Neuronal ceroid lipofuscinosis 2
Inborn genetic diseases
Autosomal recessive spinocerebellar ataxia 7
Neuronal ceroid lipofuscinosis 2
Neuronal ceroid lipofuscinosis 2
Other Variants in TPP1