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 disease and age of onset

F13A1 · rs6927354

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Sensitive

Alzheimer disease and age of onset

SYNJ1 · rs147991290

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Sensitive

Alzheimer disease and age of onset

near CST1 · rs147525344

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Sensitive

Alzheimer disease and age of onset

TMC5 · rs118099348

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Sensitive

Alzheimer disease and age of onset

near CST8 · rs113118940

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Sensitive

Alzheimer disease and age of onset

SDR42E2 · rs145049847

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Sensitive

Alzheimer disease and age of onset

TMEM132C · rs144288546

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Sensitive

Alzheimer disease and age of onset

near NRG3 · rs190780914

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Sensitive

Alzheimer disease and age of onset

near HSD17B12 · rs139675748

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Sensitive

Alzheimer disease and age of onset

near JCAD · rs146650065

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Sensitive

Alzheimer disease and age of onset

near SLC16A9 · rs61860854

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Sensitive

Alzheimer disease and age of onset

near ATP2B1 · rs117483990

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Sensitive

Alzheimer disease and age of onset

PHF14 · rs183600932

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Sensitive

Alzheimer disease and age of onset

NKAIN3 · rs4557697

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Sensitive

Alzheimer disease and age of onset

KDM1B · rs188911996

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Sensitive

Late-onset Alzheimer's disease

SLC10A2 · rs16961023

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Sensitive

Alzheimer's disease (late onset)

ABCA7 · rs115550680

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Sensitive

Dementia and core Alzheimer's disease neuropathologic changes

PVRL2 · rs6857

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Sensitive

Cerebrospinal fluid levels of Alzheimer's disease-related proteins

IL6R · rs61812598

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Sensitive

Alzheimer's disease (late onset)

SLC24A4 · rs10498633

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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.