Variants linked to Atrial Fibrillation

Continuously updated · newest added Oct 22, 2026

495 positions on this site are linked to Atrial Fibrillation, out of 106,130 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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Standard

Atrial fibrillation

SPATS2L · rs295114

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Standard

Atrial fibrillation

SPATS2L · rs3820888

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Standard

Atrial fibrillation

NEURL1 · rs55693294

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Standard

Atrial fibrillation

CFL2 · rs73241997

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Standard

Atrial fibrillation

DMRTA2 · rs56202902

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Standard

Atrial fibrillation

HAND2 · rs17059534

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Standard

Atrial fibrillation

PRRX1 · rs12142379

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Atrial fibrillation

KIF3C · rs7578393

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Standard

Atrial fibrillation

KIF3C · rs6546620

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Standard

Atrial fibrillation

PITX2 · rs17042171

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Atrial fibrillation

MYH6 · rs422068

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Atrial fibrillation

RASSF8 · rs117640426

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Standard

Atrial fibrillation

KCNN3 · rs13376333

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Atrial fibrillation

PITX2 · rs79399769

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Atrial fibrillation

NEURL1 · rs60572254

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Atrial fibrillation

XPO7 · rs7846485

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Standard

Atrial fibrillation

C9orf3 · rs4385527

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Standard

Early onset atrial fibrillation

HAND2 · rs4615152

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Atrial fibrillation

PRRX1 · rs503706

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Standard

Atrial fibrillation

KCND3 · rs12044963

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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.