Variants linked to Atrial Fibrillation

Continuously updated · newest added Oct 22, 2026

494 positions on this site are linked to Atrial Fibrillation, out of 106,046 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

MRAP-AS1 · rs2298359

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Standard

Atrial fibrillation

near GSDMB · rs7359623

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Standard

Atrial fibrillation

ZZEF1 · rs8074454

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Standard

Atrial fibrillation

CEP85L · rs9481816

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Standard

Atrial fibrillation

near LINC02750 · rs4881717

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Standard

Atrial fibrillation (MTAG)

LIN54 · rs6841049

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Standard

Atrial fibrillation (MTAG)

near VGLL2 · rs11153653

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Standard

Atrial fibrillation (MTAG)

NKAIN2 · rs563452

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Standard

Atrial fibrillation (MTAG)

FBRSL1 · rs4883571

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Standard

Atrial fibrillation (MTAG)

SMG6 · rs2209073

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Standard

Atrial fibrillation (MTAG)

RUNX1 · rs9981470

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Standard

Atrial fibrillation

near ELAVL4 · rs72688573

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Standard

Atrial fibrillation

near EPS15 · rs72661397

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Standard

Atrial fibrillation

SHISAL2A · rs148708686

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Standard

Atrial fibrillation

POM121C · rs61688923

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Standard

Atrial fibrillation

near TMEM273 · rs12253763

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Standard

Atrial fibrillation

SMG6 · rs57130712

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Standard

Atrial fibrillation

UBE2L3 · rs2266961

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Standard

Prevalent atrial fibrillation

NEURL1 · rs11598047

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Standard

Atrial fibrillation

PITX2 · rs138311480

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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.