Variants linked to Rheumatoid Arthritis

Continuously updated · newest added Oct 23, 2026

117 positions on this site are linked to Rheumatoid Arthritis, out of 112,107 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

Rheumatoid arthritis (ACPA-positive)

DDX6 · rs11217037

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Sensitive

Rheumatoid arthritis

IKZF3 · rs59716545

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Sensitive

Rheumatoid arthritis (ACPA-positive)

RCAN1 · rs2834512

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Sensitive

Rheumatoid arthritis (ACPA-positive)

STAT4 · rs13426947

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Sensitive

Rheumatoid arthritis

PLCL1 · rs6752643

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Sensitive

Rheumatoid arthritis

FIS1 · rs10275421

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Sensitive

Rheumatoid arthritis (ACPA-positive)

IRAK1 · rs13397

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Sensitive

Rheumatoid arthritis

RASGRP1 · rs8043085

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Sensitive

Rheumatoid arthritis

IRF5 · rs3778753

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Sensitive

Rheumatoid arthritis

ZBTB7C · rs8087252

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Sensitive

Rheumatoid arthritis

SDF2L1 · rs13054355

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Sensitive

Rheumatoid arthritis (ACPA-positive)

GATA3 · rs3781094

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Sensitive

Rheumatoid arthritis

BOLL · rs770667

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Sensitive

Rheumatoid arthritis (ACPA-positive)

POU3F1 · rs883220

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Sensitive

Rheumatoid arthritis (ACPA-positive)

CCR6 · rs59466457

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Sensitive

Rheumatoid arthritis

AIFM2 · rs10999147

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Sensitive

Rheumatoid arthritis

IL12RB2 · rs2201584

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Sensitive

Rheumatoid arthritis

LINC02357 · rs16878091

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Sensitive

Rheumatoid arthritis

IRAK1 · rs5987194

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Sensitive

Rheumatoid arthritis

IL20RB · rs9826828

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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.