All variants

Continuously updated · newest added Oct 22, 2026

107,852 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.

Sensitive

Chronic obstructive pulmonary disease

DPYD · rs114904431

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Standard

Educational attainment

DPYD · rs80216782

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Sensitive

Autism spectrum disorder or schizophrenia

DPYD · rs61789073

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Standard

Educational attainment

DPYD · rs28714464

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Standard

Highest math class taken (MTAG)

DPYD · rs12047563

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Standard

Height

DPYD · rs7519652

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Sensitive

Gastroesophageal reflux disease, peptic ulcer disease and/or corresponding medications and treatment

DPYD · rs61787782

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Standard

Insomnia

DPYD-IT1 · rs12725266

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Standard

Chronotype

DPYD · rs1760217

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Standard

sodium (maximum, inv-norm transformed)

DPYD · rs2811198

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Standard

Sodium (mean, inv-norm transformed)

DPYD · rs11165897

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Standard

GLIPR1 protein levels

near DPYD · rs538371550

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Standard on its own

Body mass index (MTAG)

near DPYD · rs995258

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Standard

Smoking initiation

DPYD · rs12140043

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Standard

Metabolite levels (uracil; Uracil)

DPYD · rs3790389

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Standard

Smoking initiation

DPYD · rs78542688

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Standard

Uracil levels

DPYD · rs1254152519

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Standard

Educational attainment

DPYD · rs7531138

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Standard

Educational attainment

DPYD · rs17378539

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Standard

Smoking initiation

DPYD · rs28552810

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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.