Variants linked to Alzheimer's Disease

Continuously updated · newest added Oct 25, 2026

564 positions on this site are linked to Alzheimer's Disease, out of 118,462 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

Late-onset Alzheimer's disease

near RN7SL366P · rs10806784

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Sensitive

Alzheimer's disease (MTAG)

near KRT18P16 · rs77399788

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Sensitive

Alzheimer disease and age of onset

near LINC01605 · rs188420713

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Sensitive

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

ST13P12 · rs1743330765

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Sensitive

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

near PPP1R1AP2 · rs1596645121

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Sensitive

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

KDM2A · rs1273071898

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Sensitive

Alzheimer's disease or educational attainment (pleiotropy)

EPHA1 · rs10808026

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Sensitive

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

near LINC01544 · rs140886023

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Sensitive

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

C2orf42 · rs1265024412

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Sensitive

Alzheimer's disease (MTAG)

PILRA · rs34995835

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Sensitive

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

SIL1 · rs1355274306

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Sensitive

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

ADK · rs368042471

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Sensitive

Alzheimer's disease (PheCode 290.11)

COL5A1 · rs188208995

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Sensitive

Alzheimer's disease (late onset)

EPHA1 · rs11763230

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Sensitive

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

IGSF23 · rs539159088

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Sensitive

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

MARK4 · rs34545713

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Sensitive

Alzheimer's disease, proxy Alzheimer's disease or related dementias

near RNU6-1307P · rs34450379

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Sensitive

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

CTB-179K24.3 · rs183321458

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Sensitive

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

near IPO7 · rs1590420364

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Sensitive

Alzheimer's disease (PheCode 290.11)

TBXAS1 · rs574718000

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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.