Variants linked to Alzheimer's Disease

Continuously updated · newest added Oct 25, 2026

565 positions on this site are linked to Alzheimer's Disease, out of 118,756 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Sensitive

Alzheimer's disease or related dementias

CEP89 · rs55970832

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Sensitive

Alzheimer's disease

INPP5D · rs10933431

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Sensitive

Alzheimer's disease

IDUA · rs3822030

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Sensitive

Alzheimer's disease

ANKH · rs73048837

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Sensitive

Alzheimer's disease

MME · rs61762319

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Sensitive

Alzheimer's disease or related dementias

SIGLEC11 · rs8103552

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Sensitive

Alzheimer's disease or related dementias

near SNAI1 · rs73274724

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Sensitive

Alzheimer's disease

ANKH · rs112403360

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Sensitive

Alzheimer's disease or related dementias

CASS4 · rs17462136

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Sensitive

Alzheimer's disease or related dementias

CEP89 · rs78622628

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Sensitive

Alzheimer's disease

near TRIB1 · rs115038899

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Sensitive

Alzheimer's disease

near TRIB1 · rs12544593

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Sensitive

Alzheimer's disease

MS4A6A · rs7232

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Sensitive

Alzheimer's disease

near EPHA1 · rs11769559

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Sensitive

Alzheimer's disease

PLEC · rs72695404

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Sensitive

Alzheimer's disease

SHARPIN · rs34674752

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Sensitive

Alzheimer's disease

TSPAN14 · rs7080009

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Sensitive

Alzheimer's disease

APOE · rs769450

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Sensitive

Alzheimer's disease

APOE · rs405509

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Sensitive

Alzheimer's disease or family history of Alzheimer's disease

CEACAM22P · rs75161053

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Questions about variants on this site

What is a "variant" page on this site?

One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.

Where does new variant data come from?

The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.

Does being listed here mean a variant causes a condition?

No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.

Can I search this list by gene or rsID?

Yes — the search box above matches gene symbols and rsIDs as well as trait names.