Variants linked to Atrial Fibrillation

Continuously updated · newest added Oct 22, 2026

491 positions on this site are linked to Atrial Fibrillation, out of 105,248 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

← Back to Atrial Fibrillation

Standard

Atrial fibrillation (MTAG)

near PITX2 · rs60452787

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Standard

Atrial fibrillation

LIN54 · rs13147041

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Standard

Atrial fibrillation (PheCode 427.21)

near NR3C1 · rs4501370

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Standard

Atrial fibrillation

OBSCN · rs1757148

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Standard

Atrial fibrillation

ZMIZ1-AS1 · rs58490713

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Standard

Atrial fibrillation

near ASAH1 · rs399485

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Standard

Atrial fibrillation/atrial flutter

near RNU6-1148P · rs141654122

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Standard

Atrial fibrillation

POPDC1-AS1 · rs62421401

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Standard

Atrial fibrillation

MIR1-1HG · rs13040413

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Standard

Atrial fibrillation

near OR7E161P · rs61468577

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Standard

Atrial fibrillation

MIR1-1HG · rs6062242

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Standard

Atrial fibrillation

CAMK2D · rs11938486

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Standard

Atrial fibrillation

GYPC · rs28387111

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Standard

Atrial fibrillation

near NCOR2 · rs28648976

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Standard

Atrial fibrillation

LINC02269 · rs12643389

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Standard

Atrial fibrillation

FILIP1 · rs9343292

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Standard

Atrial fibrillation

CREB5 · rs12535186

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Standard

Atrial fibrillation (MTAG)

ENPEP · rs141752220

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Standard

Atrial fibrillation

near DPF3 · rs3814866

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Standard

Atrial fibrillation

TTN-AS1 · rs3731748

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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.