All variants

Continuously updated · newest added Oct 22, 2026

108,020 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

Substance use disorder

DPYD · rs11165875

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Sensitive

Substance use disorder

DPYD · rs4950035

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Sensitive

Substance use disorder

DPYD · rs79313673

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Standard

Sleep duration (short sleep)

DPYD · rs12567114

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Standard

Sleep duration

DPYD · rs75641275

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Standard

Self-reported math ability

DPYD · rs76586805

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Standard

Educational attainment (MTAG)

DPYD · rs10875121

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Standard

Feeling nervous

DPYD · rs6703588

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Standard

Body mass index

DPYD · rs4379706

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Standard

Educational attainment (years of education)

near DPYD · rs17372140

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Sensitive

DPYD c.2846A>T — fluoropyrimidine tolerance

DPYD · rs67376798

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Sensitive

DPYD *2A — fluoropyrimidine tolerance

DPYD · rs3918290

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Sensitive

DPYD HapB3 — fluoropyrimidine tolerance

DPYD · rs75017182

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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.