Variants linked to Atrial Fibrillation

Continuously updated · newest added Oct 22, 2026

492 positions on this site are linked to Atrial Fibrillation, out of 105,416 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

TTN-AS1 · rs3731748

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Standard

Atrial fibrillation

DGKB · rs10234589

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Standard

Atrial fibrillation (MTAG)

NEURL1 · rs3781370

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Standard

Atrial fibrillation (MTAG)

near LINC01438 · rs2595082

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Standard

Atrial fibrillation

near RPL26P20 · rs56236638

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Standard

Atrial fibrillation

KCNN2 · rs2900084

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Standard

Atrial fibrillation

LINC02945 · rs180922726

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Standard

Atrial fibrillation

LINC02945 · rs145262264

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Standard

Atrial fibrillation

THRB · rs2217884

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Standard

Atrial fibrillation (MTAG)

LINC01681 · rs113116849

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Standard

Atrial fibrillation

SLC27A6 · rs72797161

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Standard

Atrial fibrillation (MTAG)

near LINC01438 · rs113832645

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Standard

Atrial fibrillation (MTAG)

near MIR297 · rs4590107

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Standard

Atrial fibrillation (MTAG)

PANCR · rs1470618

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Standard

Atrial fibrillation (MTAG)

KCNN3 · rs11264273

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Atrial fibrillation and flutter (PheCode 427.2)

ATXN1 · rs113755256

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Atrial fibrillation

SORCS3 · rs547513244

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Standard

Atrial fibrillation

LINC02269 · rs57909314

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Standard

Atrial fibrillation

WIPF1 · rs35215597

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Standard

Atrial fibrillation

near RNU1-18P · rs17084154

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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.