Variants linked to Atrial Fibrillation

Continuously updated · newest added Oct 22, 2026

495 positions on this site are linked to Atrial Fibrillation, out of 106,172 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

ZFHX3 · rs2359171

See detailed info →
Standard

Atrial fibrillation

HSPG2 · rs7529220

See detailed info →
Standard

Atrial fibrillation

SH3PXD2A · rs10509768

See detailed info →
Standard

Atrial fibrillation

PKP2 · rs12809354

See detailed info →
Standard

Atrial fibrillation

CAMK2D · rs6829664

See detailed info →
Standard

Atrial fibrillation

GORAB · rs608930

See detailed info →
Standard

Atrial fibrillation

SLC35F1 · rs17079881

See detailed info →
Standard

Atrial fibrillation

SCN10A · rs6790396

See detailed info →
Standard

Atrial fibrillation

FAM13B · rs10479177

See detailed info →
Standard

Atrial fibrillation

HCN4 · rs7164883

See detailed info →
Standard

Atrial fibrillation

CAV1/2 · rs11773845

See detailed info →
Standard

Atrial fibrillation

NEBL · rs2296610

See detailed info →
Standard

Atrial fibrillation

REEP3 · rs12245149

See detailed info →
Standard

Atrial fibrillation

KCNJ5 · rs75190942

See detailed info →
Standard

Atrial fibrillation

SLC35F1 · rs281868

See detailed info →
Standard

Atrial fibrillation

LINC01426 · rs2834618

See detailed info →
Standard

Atrial fibrillation

KCND3 · rs1545300

See detailed info →
Standard

Atrial fibrillation

CAND2 · rs7650482

See detailed info →
Standard

Atrial fibrillation

SORL1 · rs949078

See detailed info →
Standard

Atrial fibrillation

KCNN3 · rs6689306

See detailed info →

Showing 20 of 495 · page 20 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.