Variants linked to Glaucoma

Continuously updated · newest added Oct 21, 2026

446 positions on this site are linked to Glaucoma, out of 104,324 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

Intraocular pressure

SPTBN1 · rs76070960

See detailed info →
Standard

Intraocular pressure

KALRN · rs986912

See detailed info →
Standard

Intraocular pressure

PPP2R3A · rs34864445

See detailed info →
Standard

Intraocular pressure

DNALI1 · rs4653301

See detailed info →
Standard

Intraocular pressure

CPXM1 · rs34211052

See detailed info →
Standard

Intraocular pressure

KALRN · rs6776396

See detailed info →
Standard

Intraocular pressure

MECOM · rs34781085

See detailed info →
Standard

Intraocular pressure

LUM · rs57812022

See detailed info →
Standard

Intraocular pressure

FEZ2 · rs10172196

See detailed info →
Standard

Intraocular pressure

RALB · rs4549095

See detailed info →
Standard

Intraocular pressure

ISOC1 · rs11952939

See detailed info →
Standard

Intraocular pressure

TRAM2 · rs55828716

See detailed info →
Standard

Intraocular pressure

SMG6 · rs216195

See detailed info →
Standard

Intraocular pressure

CDO1 · rs34869

See detailed info →
Standard

Intraocular pressure

DNALI1 · rs2268695

See detailed info →
Standard

Intraocular pressure

STAG1 · rs13092193

See detailed info →
Standard

Intraocular pressure

ABO · rs8176741

See detailed info →
Standard

Intraocular pressure

LOC105377143 · rs4856961

See detailed info →
Standard

Intraocular pressure

RALGPS1 · rs3739555

See detailed info →
Standard

Intraocular pressure

TGFB2 · rs17047703

See detailed info →

Showing 20 of 446 · page 14 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.