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

Spherical equivalent or myopia (age of diagnosis)

TFAP2D · rs9395623

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Standard

Spherical equivalent or myopia (age of diagnosis)

LYPLAL1 · rs11118367

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Standard

Spherical equivalent or myopia (age of diagnosis)

RBFOX1 · rs10500355

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Standard

Myopia (age of diagnosis)

KCNA4 · rs534311

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Standard

Myopia (age of diagnosis)

near ZIC3 · rs1344035

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Standard

Myopia (age of diagnosis)

near H2AC12 · rs35909544

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Standard

Myopia (age of diagnosis)

near LRFN5 · rs61991628

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Standard

Myopia (age of diagnosis)

CFAP299 · rs79504986

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Standard

Myopia (age of diagnosis)

near CDRT15 · rs80253120

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Standard

Myopia (age of diagnosis)

FRMPD2 · rs11101263

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Standard

Myopia (age of diagnosis)

near ZNF280B · rs11913426

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Standard

Myopia (age of diagnosis)

ADAMTSL1 · rs7028032

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Standard

Myopia (age of diagnosis)

PLCH2 · rs10910076

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Standard

Myopia (age of diagnosis)

near PDHA1 · rs73451523

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Standard

Myopia (age of diagnosis)

CARMIL2 · rs9972635

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Standard

Myopia (age of diagnosis)

near PRL · rs411535

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Standard

Myopia (age of diagnosis)

GRM7 · rs77016368

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Standard

Myopia (age of diagnosis)

ZDHHC11 · rs6875688

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Standard

Myopia (age of diagnosis)

near AP1M1 · rs7253703

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Standard

Myopia (age of diagnosis)

NTM · rs1790165

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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.