Variants linked to Glaucoma

Continuously updated · newest added Oct 21, 2026

442 positions on this site are linked to Glaucoma, out of 103,190 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

Vertical cup-disc ratio (multi-trait analysis)

STK38 · rs72852338

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Standard

Vertical cup-disc ratio (multi-trait analysis)

GMDS · rs56031192

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Standard

Primary open angle glaucoma (multi-trait analysis)

SLC2A12 · rs2811687

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Standard

Primary open angle glaucoma (MTAG)

COL24A1 · rs6697461

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Standard

Glaucoma (primary open-angle)

APBB2 · rs59892895

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Standard

Glaucoma

near PKHD1 · rs2439041

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Standard

Primary open angle glaucoma (PheCode 365.11)

CDH11 · rs35198

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Standard

Glaucoma (primary open-angle)

TFAP2B-PKHD1 · rs2491422

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Standard

Primary open angle glaucoma (MTAG)

near XRCC6P1 · rs11187315

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Standard

Primary open angle glaucoma (PheCode 365.11)

near LTBP2 · rs2165198

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Standard

Glaucoma

ACOXL · rs11898005

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Standard

Takes medication for Glaucoma?

near CTTNBP2 · rs10264112

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Standard

Glaucoma

SMG6 · rs9891227

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Standard

Primary open angle glaucoma (multi-trait analysis)

SCFD2 · rs67349114

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Standard

Primary open angle glaucoma (PheCode 365.11)

near LINC01873 · rs1467229

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Standard

Glaucoma

LINC01641 · rs145851120

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Standard

Primary open angle glaucoma (MTAG)

SCFD2 · rs73250939

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Standard

Glaucoma

LYPLAL1-DT · rs3885898

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Standard

Glaucoma (primary open-angle)

MTOR · rs147660927

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Standard

Glaucoma

FNDC3B · rs16845236

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Showing 20 of 442 · page 5 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.