Variants linked to Glaucoma

Continuously updated · newest added Oct 21, 2026

443 positions on this site are linked to Glaucoma, out of 103,694 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

Glaucoma

ARHGEF12 · rs10790382

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Standard

Glaucoma (primary open-angle)

LYPLAL1-DT · rs6667536

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Standard

Primary open angle glaucoma (multi-trait analysis)

TFAP2B · rs3798526

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Standard

Glaucoma

near ARHGEF28P1 · rs2670338

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Standard

Primary angle-closure glaucoma (PheCode 365.2)

PCMTD1 · rs374522377

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Open-angle glaucoma (PheCode 365.1)

BNC2 · rs2149157

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Standard

Glaucoma

AFAP1 · rs16841407

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Standard

Primary open angle glaucoma (multi-trait analysis)

near PRSS23 · rs12787853

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Standard

Primary open angle glaucoma (multi-trait analysis)

near RPL21P41 · rs6795104

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Standard

Open-angle glaucoma (PheCode 365.1)

SRSF3 · rs9368943

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Standard

Glaucoma (primary open-angle)

NDP · rs17146835

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Standard

Glaucoma

near LINC00917 · rs1621350

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Standard

Primary open angle glaucoma (PheCode 365.11)

near TXNRD2 · rs34462686

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Standard

Glaucoma

TXNRD2 · rs33997573

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Primary open angle glaucoma (MTAG)

TXNRD2 · rs12158214

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Standard

Primary open angle glaucoma (MTAG)

near RPL21P41 · rs7629637

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Vertical cup-disc ratio (multi-trait analysis)

DCBLD2 · rs2880364

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Standard

Primary open angle glaucoma (MTAG)

near ME3 · rs7933920

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Standard

Glaucoma (primary open-angle)

FBXO32 · rs62521288

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Open-angle glaucoma (PheCode 365.1)

LINC01376 · rs142164320

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Showing 20 of 443 · page 7 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.