RS63750066 APP
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What This Variant Does
"rs63750066, also known as c.2137G>
Associated Conditions
Alzheimer disease type 1
Alzheimer disease
Primary degenerative dementia of the Alzheimer type
presenile onset
Cerebral amyloid angiopathy
APP-related
Alzheimer disease type 1
Alzheimer disease
Primary degenerative dementia of the Alzheimer type
presenile onset
Cerebral amyloid angiopathy
APP-related
GWAS Studies (1)
| Trait | Risk Allele | OR / Beta | P-value | Study |
|---|---|---|---|---|
| Chronic lymphocytic leukemia | — | OR: 62.24 | 2E-7 | PubMed |
Other Variants in APP