All variants

Continuously updated · newest added Sep 13, 2026

8,759 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 on its own

Takayasu arteritis

IL12B · rs4379175

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Standard on its own

Local histogram emphysema pattern

CHRNA5 · rs17486278

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Standard on its own

Local histogram emphysema pattern

MMP12 · rs17368659

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Standard

Local histogram emphysema pattern

CYP2A6 · rs56113850

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Standard on its own

Local histogram emphysema pattern

MYO1D · rs379123

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Standard on its own

Local histogram emphysema pattern

AGPHD1 · rs11852372

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Standard on its own

Lung function (forced vital capacity)

KCNJ2 · rs6501431

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Sensitive

Exfoliation glaucoma or exfoliation syndrome

TBC1D21 · rs16958445

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Standard

Age-related nuclear cataracts

CRYAA · rs11911275

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Standard

Neuroticism

near GRM3 · rs274632

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Standard on its own

Plasma homocysteine levels (post-methionine load test)

CPS1 · rs1047891

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Standard

LDL cholesterol

UGT1A1 · rs11563251

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Standard

Neuroticism

near CSMD1 · rs2407746

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Standard

Neuroticism

near PRAG1 · rs2921036

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Sensitive

Type 2 diabetes

TLE4 · rs17791513

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Standard

Serum uric acid levels

ABCG2 · rs4148152

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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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Showing 20 of 8759 · page 337 of 438

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.