Variants linked to Rheumatoid Arthritis

Continuously updated · newest added Oct 23, 2026

117 positions on this site are linked to Rheumatoid Arthritis, out of 111,939 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

PTPN2 · rs62097857

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Sensitive

Rheumatoid arthritis

TNFSF4 · rs1234313

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Sensitive

Rheumatoid arthritis

LINC02664 · rs1538981

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Sensitive

Rheumatoid arthritis

IKZF1 · rs10261758

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Sensitive

Rheumatoid arthritis

near LINC02498 · rs6831973

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Sensitive

Rheumatoid arthritis

DRAIC · rs7170107

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Sensitive

Rheumatoid arthritis

STAG1 · rs9826420

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Sensitive

Rheumatoid arthritis

CASP8 · rs2141331

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Sensitive

Rheumatoid arthritis

TNFSF4 · rs6681482

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Sensitive

Rheumatoid arthritis

LINC00824 · rs16903108

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Sensitive

Rheumatoid arthritis

GSDMB · rs56750287

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Sensitive

Rheumatoid arthritis

near NEFHP1 · rs798000

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Sensitive

Rheumatoid arthritis

near COX7CP3 · rs73005423

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Sensitive

Rheumatoid arthritis

near LINC02865 · rs7749323

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Sensitive

Rheumatoid arthritis

RASGRP1 · rs6495979

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Sensitive

Marginal zone lymphoma or rheumatoid arthritis

FBXW8 · rs16947122

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Sensitive

Rheumatoid arthritis

ILF3 · rs147622113

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Sensitive

Rheumatoid arthritis (rheumatoid factor and/or anti-cyclic citrullinated peptide seropositive)

HLA-DRB1 · rs9269234

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Sensitive

Rheumatoid arthritis

AIRE · rs2075876

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Sensitive

Rheumatoid arthritis

TNFRSF14 · rs187786174

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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.