Variants linked to Knee Osteoarthritis

Continuously updated · newest added Oct 23, 2026

128 positions on this site are linked to Knee Osteoarthritis, out of 112,527 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 Knee Osteoarthritis

Sensitive

Knee osteoarthritis

ZFP64 · rs75478182

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Sensitive

Knee osteoarthritis

LINC02796 · rs2568956

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Sensitive

Knee osteoarthritis

MAML2 · rs10831476

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Sensitive

Body mass index or knee osteoarthritis (pleiotropy)

WSCD2 · rs35739367

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Sensitive

Osteoarthritis

TPPP · rs11749927

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Sensitive

Knee osteoarthritis

AMPD3 · rs11042731

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Sensitive

Osteoarthritis

FARP2 · rs62190411

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Sensitive

Body mass index or knee osteoarthritis (pleiotropy)

near C20orf181 · rs56103247

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Sensitive

Knee osteoarthritis

LINC02982 · rs55658362

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Sensitive

Knee osteoarthritis

SLC25A13 · rs12155373

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Sensitive

Body mass index or knee osteoarthritis (pleiotropy)

near MAFB · rs6029202

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Sensitive

Knee osteoarthritis

PTCH1 · rs79057214

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Sensitive

Osteoarthritis

near PDPR · rs62052494

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Sensitive

Knee osteoarthritis

ATG7 · rs2443701

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Sensitive

Osteoarthritis

near TNPO3P2 · rs62405439

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Sensitive

Idiopathic knee osteoarthritis

C19orf38 · rs12978481

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Sensitive

Knee osteoarthritis

LINC02182 · rs12925886

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Sensitive

Osteoarthritis

near TMEM18 · rs35628463

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Sensitive

Osteoarthritis

SMG6 · rs216175

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Sensitive

Knee osteoarthritis

near RNU6-543P · rs10995385

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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.