All variants

Continuously updated · newest added Oct 21, 2026

102,854 variants MyGeneLog™ checks for — each with its own plain-language page and cited source. New findings are collected from the public GWAS Catalog every twenty minutes.

Standard

Triglycerides

APOE · rs115299243

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Standard

Cholesterol efflux capacity (BHK stimulated assay)

APOE/C1/C2/C4 · rs141622900

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Standard

Cerebral amyloid deposition (PET imaging)

APOE · rs10414043

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Standard

Cerebral amyloid deposition (PET imaging)

APOC1 · rs12721046

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Standard

Cerebral amyloid deposition (PET imaging)

APOE · rs438811

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Standard

Cerebral amyloid deposition (PET imaging)

TOMM40 · rs71352238

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Standard

Cerebral amyloid deposition (PET imaging)

APOE · rs483082

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Standard

Cerebral amyloid deposition (PET imaging)

PVRL2 · rs12972970

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Standard

Cerebral amyloid deposition (PET imaging)

TOMM40 · rs34095326

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Standard

Cerebral amyloid deposition (PET imaging)

TOMM40 · rs184017

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Standard

Cerebral amyloid deposition (PET imaging)

TOMM40 · rs10119

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Standard

Cerebral amyloid deposition (PET imaging)

TOMM40 · rs157582

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Standard

Cerebral amyloid deposition (PET imaging)

PVRL2 · rs283815

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Sensitive

Alzheimer's disease in APOE e4- carriers

near USP6NL · rs11257238

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Standard

Cerebrospinal T-tau levels

APOE · rs769449

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Standard

Cholesterol, total

APOE · rs7412

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Standard

Resting heart rate

APOE · rs12721051

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Sensitive

Lewy body disease

APOE · rs429358

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Standard

LDL cholesterol

APOE · rs4420638

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Sensitive

Alzheimer's disease (late onset)

APOE · rs2075650

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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.