Variants linked to Atrial Fibrillation

Continuously updated · newest added Oct 22, 2026

493 positions on this site are linked to Atrial Fibrillation, out of 105,752 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

PRKD1 · rs17115113

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Standard

Atrial fibrillation (MTAG)

ARHGAP10 · rs6839459

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Standard

Atrial fibrillation

GRB10 · rs2529415

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Standard

Atrial fibrillation

near MIR30B · rs72721963

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Standard

Atrial fibrillation

UBR5 · rs2168689

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Standard

Atrial fibrillation

near DAPK3 · rs141278070

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Atrial fibrillation

near RBMS1 · rs4368343

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Standard

Atrial fibrillation

DTNA · rs1790534

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Standard

Atrial fibrillation (MTAG)

LINC02269 · rs74500426

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Atrial fibrillation and flutter (PheCode 427.2)

CCDC136 · rs17165121

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Standard

Atrial fibrillation

near ACVR2A · rs4972357

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Standard

Atrial fibrillation (PheCode 427.21)

CPEB4 · rs17694835

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Standard

Atrial fibrillation

PIK3CD · rs138766815

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Standard

Atrial fibrillation

near PDPR · rs183692602

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Standard

Atrial fibrillation

NEK6 · rs10818943

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Standard

Atrial fibrillation (PheCode 427.21)

WIPF1 · rs4378760

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Standard

Atrial fibrillation

CUX1 · rs2158902

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Standard

Atrial fibrillation

AMZ1 · rs798514

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Standard

Atrial fibrillation

CYS1 · rs56242692

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Standard

Atrial fibrillation

ABLIM1 · rs17719358

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Showing 20 of 493 · page 13 of 25

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.