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 118,864 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

near SPDYE3 · rs7384878

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Sensitive

Alzheimer's disease or related dementias

DOCK4 · rs144867634

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Sensitive

Alzheimer's disease or related dementias

RASGEF1C · rs113706587

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Sensitive

Alzheimer's disease or related dementias

TMEM106B · rs5011438

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Sensitive

Alzheimer's disease or related dementias

near HLA-DQB1 · rs9275207

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Sensitive

Alzheimer's disease or related dementias

near NME8 · rs2167266

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Sensitive

Alzheimer's disease or related dementias

ATP8B4 · rs183428733

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Sensitive

Alzheimer's disease or related dementias

FERMT2 · rs17125944

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Sensitive

Alzheimer's disease or related dementias

ATP8B4 · rs138799625

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Sensitive

Alzheimer's disease or related dementias

RIC8B · rs7977765

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Sensitive

Alzheimer's disease or related dementias

GTF2H3 · rs34996665

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Sensitive

Alzheimer's disease or related dementias

near EED · rs10792831

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Sensitive

Alzheimer's disease or related dementias

FERMT2 · rs17125924

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Sensitive

Alzheimer's disease or related dementias

ABCA7 · rs113767014

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Sensitive

Alzheimer's disease or related dementias

ABCA7 · rs4147918

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Sensitive

Alzheimer's disease or related dementias

near ADAMTS1 · rs3017432

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Sensitive

Alzheimer's disease

near NCK2 · rs112538822

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Sensitive

Alzheimer's disease

near CYP27C1 · rs1983088

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Sensitive

Alzheimer's disease

NCK2 · rs143080277

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Sensitive

Alzheimer's disease or related dementias

near SIGLEC11 · rs875121

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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.