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 118,378 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 family history of Alzheimer's disease

near PIK3CD · rs1644420296

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Sensitive

Alzheimer's disease in APOE e44 or e43 genotype

HP1BP3 · rs2274119

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Sensitive

Alzheimer's disease in APOE e33 genotype

NPAS3 · rs187023552

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Sensitive

Alzheimer's disease in APOE e33 or e44 or e43 genotype

USP3 · rs77892656

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Sensitive

Alzheimer's disease in APOE e44 or e43 genotype

DDHD1-DT · rs10131116

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Sensitive

Alzheimer's disease in APOE e33 genotype

HLA-DRB9 · rs9268888

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Sensitive

Alzheimer's disease in APOE e44 or e43 genotype

CASS4 · rs113221226

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Sensitive

Alzheimer's disease in APOE e44 or e43 genotype

near TSBP1-AS1 · rs17208902

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Sensitive

Alzheimer's disease in APOE e44 or e43 genotype

APH1B · rs75763893

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Sensitive

Rate of cognitive decline in Alzheimer's disease

SCN2A · rs111535588

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Sensitive

Alzheimer's disease or educational attainment (pleiotropy)

KCNH1 · rs61848607

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Sensitive

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

ZNF385B · rs367921783

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Sensitive

Alzheimer's disease or educational attainment (pleiotropy)

CHST10 · rs2241809

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Sensitive

Rate of cognitive decline in Alzheimer's disease

LINC02668 · rs148405458

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Sensitive

Alzheimer's disease or educational attainment (pleiotropy)

STAU1 · rs141979783

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Sensitive

Alzheimer's disease, proxy Alzheimer's disease or related dementias in APOE e4 non-carriers

near TSPEAR · rs139130053

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Sensitive

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

TMEM163 · rs10164986

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Sensitive

Rate of cognitive decline in Alzheimer's disease

near LINC02039 · rs78049001

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Sensitive

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

STAG3 · rs4727449

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Sensitive

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

SNX6 · rs376690477

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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.