Gene Knowledge Graph
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Variants linked to Glaucoma

Continuously updated · newest added Oct 21, 2026

439 positions on this site are linked to Glaucoma, out of 102,854 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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Standard

Primary open angle glaucoma (multi-trait analysis)

KALRN · rs10512626

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Primary open angle glaucoma (MTAG)

LINC02687 · rs10160502

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Primary open angle glaucoma (MTAG)

near ERG · rs994003

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Vertical cup-disc ratio (multi-trait analysis)

IRS2 · rs9521601

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Primary open angle glaucoma (multi-trait analysis)

STOX2 · rs35770501

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Primary open angle glaucoma (multi-trait analysis)

TESK2 · rs9429072

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Primary open angle glaucoma (MTAG)

near RPL23AP48 · rs9320840

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Vertical cup-disc ratio (multi-trait analysis)

PPP1R36 · rs28761289

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Primary open angle glaucoma (MTAG)

near SLC2A12 · rs2811680

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Vertical cup-disc ratio (multi-trait analysis)

ABO · rs8176662

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Glaucoma (low intraocular pressure)

GMDS · rs62391632

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Primary open angle glaucoma (PheCode 365.11)

ME3 · rs60229086

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Primary open angle glaucoma (multi-trait analysis)

near HMGB1P46 · rs3019951

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Primary open angle glaucoma (PheCode 365.11)

ARHGAP20 · rs11213533

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Primary open angle glaucoma (MTAG)

near MYO16 · rs9587617

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Open-angle glaucoma (PheCode 365.1)

SASH1 · rs73015038

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Primary open angle glaucoma (PheCode 365.11)

MLLT3 · rs4007655

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Primary open angle glaucoma (multi-trait analysis)

near ITGB3 · rs2317385

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Open-angle glaucoma (PheCode 365.1)

PELO-AS1 · rs141502740

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Vertical cup-disc ratio (adjusted for vertical disc diameter)

RIC8B · rs9651957

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Showing 20 of 439 · page 3 of 22

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.