Variants linked to Atrial Fibrillation

Continuously updated · newest added Oct 21, 2026

490 positions on this site are linked to Atrial Fibrillation, out of 105,038 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

FAM13B · rs10479177

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Atrial fibrillation

SCN10A · rs6790396

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Atrial fibrillation

SLC35F1 · rs17079881

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Atrial fibrillation

FBXO32 · rs78332318

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Atrial fibrillation

GORAB · rs608930

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Atrial fibrillation

PKP2 · rs12809354

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Atrial fibrillation

LINC00477 · rs10842383

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Atrial fibrillation

SLIT3 · rs12188351

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Atrial fibrillation

ERBB4 · rs35544454

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Atrial fibrillation

KCND3 · rs1443926

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Atrial fibrillation

ARNT2 · rs12908004

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Atrial fibrillation

KCND3 · rs12044963

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Atrial fibrillation

WNT8A · rs2040862

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Atrial fibrillation

PRRX1 · rs503706

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Early onset atrial fibrillation

HAND2 · rs4615152

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Atrial fibrillation

C9orf3 · rs4385527

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Atrial fibrillation

NEURL1 · rs60572254

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Atrial fibrillation

NUCKS1 · rs951366

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Atrial fibrillation

PITX2 · rs79399769

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Atrial fibrillation

KCNN3 · rs13376333

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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.