Variants linked to Glaucoma

Continuously updated · newest added Oct 21, 2026

440 positions on this site are linked to Glaucoma, out of 103,022 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 (multi-trait analysis)

PKHD1 · rs6458804

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Standard

Primary open angle glaucoma (multi-trait analysis)

near LINC01948 · rs184992

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Standard

Glaucoma (primary open-angle)

near CTTNBP2 · rs13438572

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Standard

Primary open angle glaucoma (multi-trait analysis)

ANGPT1 · rs41420946

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Standard

Primary open angle glaucoma (multi-trait analysis)

LOXL1 · rs2415204

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Standard

Primary open angle glaucoma (MTAG)

EFEMP1 · rs17047290

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Standard

Glaucoma (primary open-angle)

GTF2E2 · rs13268581

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Standard

Glaucoma (primary open-angle)

LOXL1-AS1 · rs8034017

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Standard

Primary open angle glaucoma (MTAG)

near METTL15 · rs7931440

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Standard

Primary open angle glaucoma (multi-trait analysis)

GMDS · rs75570691

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Standard

Primary open angle glaucoma (MTAG)

near COL8A1 · rs73134321

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Standard

Primary open angle glaucoma (multi-trait analysis)

near LINC02379 · rs6534524

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Standard

Primary open angle glaucoma (multi-trait analysis)

GAS7 · rs3786080

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Standard

Glaucoma (high intraocular pressure)

ARHGEF12 · rs1812974

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Standard

Primary open angle glaucoma (MTAG)

near HMGB1P46 · rs141601750

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Standard

Glaucoma (primary open-angle)

GMDS · rs12664587

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Standard

Glaucoma (primary open-angle)

CYP26A1 · rs10882167

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Standard

Glaucoma (primary angle closure)

near SEMA3A · rs10215636

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Standard

Primary open angle glaucoma (multi-trait analysis)

near SCARF2 · rs10212080

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Standard

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

ABI3BP · rs9827694

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Showing 20 of 440 · page 1 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.