RS138976576 TPP1
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Associated Conditions
Neuronal ceroid lipofuscinosis 2
Autosomal recessive spinocerebellar ataxia 7
Inborn genetic diseases
Neuronal ceroid lipofuscinosis 2
Autosomal recessive spinocerebellar ataxia 7
Inborn genetic diseases
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| TPP1 protein levels | T | OR: 0.99 | 3E-39 | PubMed |
Other Variants in TPP1