Variants linked to Atrial Fibrillation

Continuously updated · newest added Oct 22, 2026

494 positions on this site are linked to Atrial Fibrillation, out of 105,962 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

CDK6 · rs7804722

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Atrial fibrillation

FAF1 · rs56323917

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Atrial fibrillation (PheCode 427.21)

near LINC01438 · rs17042059

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Atrial fibrillation

MAP3K3 · rs3785574

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Atrial fibrillation

RPL7 · rs7819550

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Atrial fibrillation

SHROOM3 · rs4447885

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Atrial fibrillation

near SORL1 · rs7946552

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Atrial fibrillation and flutter (PheCode 427.2)

near RN7SL734P · rs56059557

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Atrial fibrillation

MICU2 · rs11841562

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Atrial fibrillation

NAV2 · rs4757877

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Atrial fibrillation

EPHA3 · rs11921985

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Atrial fibrillation

LRMDA · rs10458662

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Atrial fibrillation and flutter (PheCode 427.2)

NAV2 · rs1442714

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Atrial fibrillation and flutter (PheCode 427.2)

TTN · rs62178975

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Atrial fibrillation

KCNH2 · rs3778872

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Atrial fibrillation

KCND3 · rs2120436

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Atrial fibrillation

LINC02269 · rs55850202

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Atrial fibrillation

XPO7 · rs17060685

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Atrial fibrillation

near NR3C1 · rs11741656

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Atrial fibrillation

TTN · rs890578

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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.