All Variants

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.

Body mass index

QT interval

Feeling miserable

Primary biliary cholangitis

Menarche (age at onset)

Menarche (age at onset)

Menarche (age at onset)

Complement C3 and C4 levels

Complement C3 and C4 levels

Complement C3 and C4 levels

C-reactive protein levels

C-reactive protein levels

LDL cholesterol

Rheumatoid arthritis

Homocysteine levels

Bladder cancer

Crohn's disease

Hemoglobin

Electrocardiographic traits

Glaucoma

Questions about variants on this site