Variants linked to Atrial Fibrillation

Continuously updated · newest added Oct 21, 2026

490 positions on this site are linked to Atrial Fibrillation, out of 105,038 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 (MTAG)

CEP85L · rs62424001

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Standard

Atrial fibrillation

near SPAM1 · rs12671215

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Standard

Atrial fibrillation

RRAGC-DT · rs6600279

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Standard

Atrial fibrillation

PTPRS · rs2613813

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Standard

Atrial fibrillation (MTAG)

near STN1 · rs12220140

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Standard

Atrial fibrillation

ZNF831 · rs77044088

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Standard

Atrial fibrillation (MTAG)

CAV2-DT · rs11974466

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Standard

Atrial fibrillation (PheCode 427.21)

near GJA8 · rs114158239

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Standard

Atrial fibrillation

HLTF-AS1 · rs4377452

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Standard

Atrial fibrillation

near SPAM1 · rs112274198

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Standard

Atrial fibrillation

ATP5F1AP3 · rs144630651

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Standard

Atrial fibrillation and flutter (PheCode 427.2)

PTGES3 · rs10747769

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Standard

Atrial fibrillation

LINC02945 · rs188987157

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Standard

Atrial fibrillation

SMARCAD1-DT · rs2865341

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Standard

Atrial fibrillation

JPH2 · rs1014754

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Standard

Atrial fibrillation

TMEM30A-DT · rs77313832

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Standard

Atrial fibrillation

HSPA9 · rs41295699

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Standard

Atrial fibrillation

SLC16A12 · rs112307214

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Standard

Atrial fibrillation

SLC16A12 · rs111288780

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Standard

Atrial fibrillation

near PRKG2 · rs1443541

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Showing 20 of 490 · page 7 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.