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 (MTAG)

CEACAM16-AS1 · rs79638902

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Sensitive

Alzheimer's disease (MTAG)

near NECTIN2 · rs28615360

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Sensitive

Alzheimer's disease (MTAG)

RELB · rs35255921

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Sensitive

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

near IGHV3-64 · rs56965016

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Sensitive

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

snoZ6 · rs150820726

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Sensitive

Alzheimer's disease (age of onset)

ADRA1B · rs62377696

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Sensitive

Alzheimer's disease (age of onset)

CD2AP · rs9395285

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Sensitive

Alzheimer's disease (age of onset)

near TAS2R60 · rs9640386

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Sensitive

Alzheimer's disease (age of onset)

near ECHDC3 · rs7920721

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Sensitive

Alzheimer's disease (age of onset)

LDLRAD4 · rs1284402

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Sensitive

Alzheimer's disease

near BIN1 · rs12989701

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Sensitive

Alzheimer's disease

near BIN1 · rs13009551

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Sensitive

Alzheimer's disease

DYM · rs138229840

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Sensitive

Alzheimer's disease

DYM · rs142978359

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Sensitive

Alzheimer's disease

TOMM40 · rs144618582

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Sensitive

Alzheimer's disease

NECTIN2 · rs145654351

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Sensitive

Alzheimer's disease

TOMM40 · rs148998607

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Sensitive

Alzheimer's disease

MOB1A · rs150214656

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Sensitive

Alzheimer's disease

near APOC1 · rs157591

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Sensitive

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

RAP1GAP2 · rs1031320110

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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.