Variants linked to Atrial Fibrillation

Continuously updated · newest added Oct 21, 2026

488 positions on this site are linked to Atrial Fibrillation, out of 104,702 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

near YWHAE · rs61248729

See detailed info →
Standard

Atrial fibrillation

EEFSEC · rs56287882

See detailed info →
Standard

Atrial fibrillation

near TNRC6A · rs12924246

See detailed info →
Standard

Atrial fibrillation (MTAG)

HAND2-AS1 · rs11933956

See detailed info →
Standard

Atrial fibrillation and flutter (PheCode 427.2)

ENPEP · rs192833524

See detailed info →
Standard

Atrial fibrillation

AGPAT1 · rs17493811

See detailed info →
Standard

Atrial fibrillation

near RNU6-367P · rs17076376

See detailed info →
Standard

Atrial fibrillation

near TBC1D32 · rs6941079

See detailed info →
Standard

Atrial fibrillation

near TBC1D32 · rs77190117

See detailed info →
Standard

Atrial fibrillation (MTAG)

PRRX1 · rs76074817

See detailed info →
Standard

Atrial fibrillation

CIAO3 · rs9928077

See detailed info →
Standard

Atrial fibrillation

near LINC01752 · rs8126119

See detailed info →
Standard

Atrial fibrillation/atrial flutter

PKP2 · rs34791177

See detailed info →
Standard

Atrial fibrillation

HDAC5 · rs170637

See detailed info →
Standard

Atrial fibrillation

XRN1 · rs11714244

See detailed info →
Standard

Atrial fibrillation

CREB5 · rs9639575

See detailed info →
Standard

Atrial fibrillation

LINC02615 · rs6849689

See detailed info →
Standard

Atrial fibrillation

CASC15 · rs3734215

See detailed info →
Standard

Atrial fibrillation

TWIST1 · rs28572114

See detailed info →
Standard

Atrial fibrillation

H1-10-AS1 · rs62266924

See detailed info →

Showing 20 of 488 · page 2 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.