Variants linked to Systemic Lupus Erythematosus

Continuously updated · newest added Oct 23, 2026

709 positions on this site are linked to Systemic Lupus Erythematosus, out of 111,393 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Sensitive

Systemic lupus erythematosus

IRF5 · rs35000415

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Sensitive

Systemic lupus erythematosus

STAT4 · rs6736175

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Sensitive

Systemic lupus erythematosus

IRF8 · rs13332649

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Sensitive

Systemic lupus erythematosus

UBE2L3 · rs3747093

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Sensitive

Systemic lupus erythematosus

PRDM1 · rs6568431

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Sensitive

Systemic lupus erythematosus

IRF7 · rs58688157

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Sensitive

Systemic lupus erythematosus

TYK2 · rs11085727

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Sensitive

Systemic lupus erythematosus

TCF7 · rs4388254

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Sensitive

Systemic lupus erythematosus

TNIP1 · rs6889239

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Sensitive

Systemic lupus erythematosus

SMG7 · rs17849501

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Sensitive

Systemic lupus erythematosus

IRF5 · rs3757387

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Sensitive

Systemic lupus erythematosus

FCGR2A · rs6671847

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Sensitive

Systemic lupus erythematosus

CSK · rs2289583

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Sensitive

Systemic lupus erythematosus

IRF5 · rs729302

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Sensitive

Systemic lupus erythematosus

DGUOK · rs4852324

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Sensitive

Systemic lupus erythematosus

DGUOK · rs6705628

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Sensitive

Systemic lupus erythematosus

CDKN1B · rs34330

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Sensitive

Systemic lupus erythematosus

CD80 · rs6804441

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Sensitive

Systemic lupus erythematosus

STAT4 · rs11889341

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Sensitive

Systemic lupus erythematosus

HLA-DQB1 · rs114092478

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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.