Variants linked to Glaucoma

Continuously updated · newest added Oct 21, 2026

444 positions on this site are linked to Glaucoma, out of 104,072 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 Glaucoma

Standard

Primary open angle glaucoma (MTAG)

COL4A1 · rs61963301

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Standard

Glaucoma (primary angle closure)

DPM2 · rs3739821

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Standard

Vertical cup-disc ratio (multi-trait analysis)

FLRT2 · rs984586

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Standard

Primary open angle glaucoma (MTAG)

near ZC3H11B · rs78359867

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Standard

Glaucoma

near PKHD1 · rs2495850

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Standard

Glaucoma

PRICKLE2 · rs13326797

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Standard

Primary open angle glaucoma (multi-trait analysis)

ACOXL · rs9308689

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Standard

Glaucoma (primary open-angle)

FNDC3B · rs62283809

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Standard

Glaucoma

KIAA1549L · rs34828249

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Standard

Glaucoma

near FBXO32 · rs62521292

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Standard

Primary open angle glaucoma (multi-trait analysis)

AFAP1 · rs4689872

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Standard

Primary open angle glaucoma (multi-trait analysis)

GLIS1 · rs11206194

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Standard

Primary open angle glaucoma (multi-trait analysis)

MECOM · rs13090630

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Standard

Glaucoma

near PKIA-AS1 · rs9643733

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Standard

Glaucoma

RFX4 · rs11113070

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Standard

Primary open angle glaucoma (multi-trait analysis)

LINC03082 · rs2218471

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Standard

Primary open angle glaucoma (multi-trait analysis)

near LINC02131 · rs280875

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Standard

Glaucoma

PDZD2 · rs72759618

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Standard

Primary open angle glaucoma (MTAG)

near RN7SKP155 · rs17254069

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Standard

Primary open angle glaucoma (multi-trait analysis)

near MIR4778 · rs4414666

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Showing 20 of 444 · page 10 of 23

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.