All variants

Continuously updated · newest added Sep 16, 2026

12,425 variants MyGeneLog™ checks for — each with its own plain-language page and cited source. New findings are collected from the public GWAS Catalog every twenty minutes.

Standard

LDL cholesterol

UGT1A1 · rs11563251

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Standard on its own

Lung function (forced vital capacity)

KCNJ2 · rs6501431

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Standard on its own

Bone properties (heel)

GPATCH1 · rs10416265

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Sensitive

Rheumatoid arthritis

CCR6 · rs1854853

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Standard on its own

Bone properties (heel)

ESR1 · rs2982552

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Standard

HDL cholesterol

DAGLB · rs702485

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Standard

Primary tooth development (number of teeth)

IGF2BP1 · rs1994969

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Standard

Primary tooth development (number of teeth)

CACNB2 · rs10740993

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Sensitive

Cystic fibrosis-related diabetes

SLC26A9 · rs4077468

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Standard

Primary tooth development (number of teeth)

AJUBA · rs997154

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Standard

White blood cell count (basophil)

near CEBPA · rs10401672

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Standard

Primary tooth development (number of teeth)

CALU · rs1799922

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Sensitive

Breast cancer

TET2 · rs9790517

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Sensitive

Breast cancer

ITPR1 · rs6762644

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Standard

Corneal structure

LPAR1 · rs1007000

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Standard

Corneal structure

CHSY1 · rs752092

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Standard

Corneal structure

TJP1 · rs785422

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Standard

Corneal structure

FOXO1 · rs2721051

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Sensitive

Breast cancer

DIRC3 · rs16857609

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Sensitive

Breast cancer

METAP1D · rs2016394

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Showing 20 of 12425 · page 521 of 622

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.