Variants linked to Atrial Fibrillation

Continuously updated · newest added Oct 21, 2026

490 positions on this site are linked to Atrial Fibrillation, out of 104,870 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

KDM2B · rs12423334

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Standard

Atrial fibrillation

near RN7SL311P · rs7654084

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Standard

Atrial fibrillation

near LSM6 · rs6821444

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Standard

Atrial fibrillation

SYNE3 · rs61983373

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Standard

Atrial fibrillation (MTAG)

GORAB-AS1 · rs1333135

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Standard

Atrial fibrillation

near LINC01376 · rs55709426

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Standard

Atrial fibrillation

TEX41 · rs1438897

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Standard

Atrial fibrillation

MYO6 · rs12211167

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Standard

Atrial fibrillation (MTAG)

ENPEP · rs28705758

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Standard

Atrial fibrillation

SMARCAD1 · rs17309887

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Standard

Atrial fibrillation

ZNF516 · rs112984554

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Standard

Atrial fibrillation (MTAG)

near RNU6-289P · rs72674110

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Standard

Atrial fibrillation

RHBDL2 · rs61750827

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Standard

Atrial fibrillation

MBTD1 · rs11870136

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Standard

Atrial fibrillation

CAPZB · rs10917449

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Standard

Atrial fibrillation

SPON1 · rs10500790

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Standard

Atrial fibrillation

ZNF516 · rs9954310

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Standard

Atrial fibrillation

ZBTB17 · rs848189

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Standard

Atrial fibrillation

DTX2P1-UPK3BP1-PMS2P11 · rs4406337

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Standard

Atrial fibrillation

DTNA · rs1954861

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Showing 20 of 490 · page 5 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.