Variants linked to Myopia

Continuously updated · newest added Sep 13, 2026

95 positions on this site are linked to Myopia, out of 9,061 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 Myopia

Standard

Myopia (age of diagnosis)

near VPREB1 · rs7286621

See detailed info →
Standard

Myopia (age of diagnosis)

C8orf44-SGK3 · rs2272774

See detailed info →
Standard

Myopia (OPN1LW exon-3 haplotype)

OPN1LW · rs145009674

See detailed info →
Standard

Spherical equivalent (joint analysis main effects and education interaction)

MYO1D-TMEM98 · rs72483203

See detailed info →
Standard

Spherical equivalent (joint analysis main effects and education interaction)

KCNJ2 · rs929474

See detailed info →
Standard

Spherical equivalent (joint analysis main effects and education interaction)

A2BP1 · rs6500957

See detailed info →
Standard

Spherical equivalent (joint analysis main effects and education interaction)

RASGRF1 · rs6495367

See detailed info →
Standard

Spherical equivalent (joint analysis main effects and education interaction)

DIS3L-MAP2K1 · rs16949788

See detailed info →
Standard

Spherical equivalent (joint analysis main effects and education interaction)

AREG · rs12511037

See detailed info →
Standard

Spherical equivalent (joint analysis main effects and education interaction)

BICC1 · rs1649081

See detailed info →
Standard

Spherical equivalent (joint analysis main effects and education interaction)

TJP2 · rs11145488

See detailed info →
Standard

Spherical equivalent (joint analysis main effects and education interaction)

TOX · rs10089517

See detailed info →
Standard

Spherical equivalent (joint analysis main effects and education interaction)

SLC14A2 · rs10853531

See detailed info →
Standard

Myopia (severe)

SNTB1 · rs6469937

See detailed info →
Standard

Myopia (pathological)

MIPEP · rs9318086

See detailed info →

Showing 15 of 95 · page 5 of 5

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.