Variants linked to Exostosis of Jaw

Continuously updated · newest added Oct 18, 2026

25 positions on this site are linked to Exostosis of Jaw, out of 91,357 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 Exostosis of Jaw

Standard

Exostosis of jaw (PheCode 526.8)

near LINC02903 · rs538989321

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Standard

Exostosis of jaw (PheCode 526.8)

near NUP58P1 · rs535192512

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Standard

Exostosis of jaw (PheCode 526.8)

near EVX2 · rs184519785

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Standard

Exostosis of jaw (PheCode 526.8)

near RPL38P2 · rs181483238

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Standard

Exostosis of jaw (PheCode 526.8)

ELOVL5 · rs142726098

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Standard

Exostosis of jaw (PheCode 526.8)

NETO1 · rs572272840

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Standard

Exostosis of jaw (PheCode 526.8)

ZFPM2 · rs559322533

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Standard

Exostosis of jaw (PheCode 526.8)

near OR2T3 · rs142690927

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Standard

Exostosis of jaw (PheCode 526.8)

CRYBG1 · rs111829969

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Standard

Exostosis of jaw (PheCode 526.8)

LINC03019 · rs140861916

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Standard

Exostosis of jaw (PheCode 526.8)

DDC · rs145505700

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Standard

Exostosis of jaw (PheCode 526.8)

LINC02819 · rs139575989

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Standard

Exostosis of jaw (PheCode 526.8)

MFF · rs575997043

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Standard

Exostosis of jaw (PheCode 526.8)

KCTD8 · rs556962187

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Standard

Exostosis of jaw (PheCode 526.8)

LINC02873 · rs149729817

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Standard

Exostosis of jaw (PheCode 526.8)

near FTH1P7 · rs374462308

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Standard

Exostosis of jaw (PheCode 526.8)

AOX2P · rs146418869

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Standard

Exostosis of jaw (PheCode 526.8)

near MIR1202 · rs187052602

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Standard

Exostosis of jaw (PheCode 526.8)

PRKN · rs182756278

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Standard

Exostosis of jaw (PheCode 526.8)

PWRN1 · rs577272962

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Showing 20 of 25 · page 1 of 2

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.