Variants linked to Atrial Fibrillation

Continuously updated · newest added Oct 21, 2026

487 positions on this site are linked to Atrial Fibrillation, out of 104,534 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/atrial flutter

near SEPTIN6 · rs77806999

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Standard

Atrial fibrillation

RNF40 · rs72793383

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Standard

Atrial fibrillation

BAIAP2 · rs72634328

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Standard

Atrial fibrillation (MTAG)

ENPEP · rs524788

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Standard

Atrial fibrillation

near TBX20 · rs2075125

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Standard

Atrial fibrillation

near UQCRHP1 · rs150043706

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Standard

Atrial fibrillation

AK9 · rs10457194

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Standard

Atrial fibrillation

PHACTR2 · rs7741998

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Standard

Atrial fibrillation (MTAG)

KCNN3 · rs1218550

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Standard

Atrial fibrillation

near FAT3 · rs11019860

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Standard

Atrial fibrillation

near U8 · rs10910469

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Standard

Atrial fibrillation (MTAG)

LINC01681 · rs7415755

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Standard

Atrial fibrillation

MBNL2 · rs7333641

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Standard

Atrial fibrillation/atrial flutter

SPON1 · rs7116230

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Standard

Atrial fibrillation

LINC01572 · rs60962205

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Standard

Atrial fibrillation

near TIAL1P1 · rs2397026

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Standard

Atrial fibrillation

near LINC01450 · rs10441103

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Standard

Atrial fibrillation

CCDC26 · rs79164994

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Standard

Atrial fibrillation

TUT7 · rs700771

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Standard

Atrial fibrillation

near YWHAE · rs61248729

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Showing 20 of 487 · page 1 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.