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.

← Back to Alzheimer's Disease

Sensitive

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

PVRL2 · rs138607350

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Sensitive

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

CNTNAP2 · rs114360492

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Sensitive

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

HESX1 · rs184384746

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Sensitive

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

BCAM · rs28399637

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Sensitive

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

MS4A6A · rs983392

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Sensitive

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

TREM2 · rs187370608

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Sensitive

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

HLA-DRB1 · rs6931277

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Sensitive

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

APH1B · rs117618017

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Sensitive

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

INPP5D · rs35349669

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Sensitive

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

SCIMP · rs113260531

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Sensitive

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

ALPK2 · rs76726049

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Sensitive

Alzheimer's disease (late onset)

ATP5C1 · rs139967528

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Sensitive

Alzheimer's disease in APOE e4- carriers

near USP6NL · rs11257238

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Sensitive

Alzheimer disease and age of onset

near METAP1 · rs115809613

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Sensitive

Alzheimer disease and age of onset

GABRA2 · rs147028191

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Sensitive

Alzheimer disease and age of onset

PTPRG · rs7609954

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Sensitive

Alzheimer disease and age of onset

near FBXO8 · rs76930906

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Sensitive

Alzheimer disease and age of onset

near PAPOLG · rs115291397

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Sensitive

Alzheimer disease and age of onset

OSBPL6 · rs1347297

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Sensitive

Alzheimer disease and age of onset

ITSN2 · rs75009721

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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.