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.

Ischemic stroke

Systolic blood pressure

Systolic blood pressure

Bone mineral density (spine)

Systolic blood pressure

Systolic blood pressure

Night sleep phenotypes

C-reactive protein levels or triglyceride levels (pleiotropy)

C-reactive protein levels or total cholesterol levels (pleiotropy)

C-reactive protein levels or total cholesterol levels (pleiotropy)

C-reactive protein levels or total cholesterol levels (pleiotropy)

C-reactive protein levels or total cholesterol levels (pleiotropy)

C-reactive protein levels or total cholesterol levels (pleiotropy)

C-reactive protein levels or triglyceride levels (pleiotropy)

C-reactive protein levels or triglyceride levels (pleiotropy)

C-reactive protein levels or triglyceride levels (pleiotropy)

C-reactive protein levels or triglyceride levels (pleiotropy)

C-reactive protein levels or triglyceride levels (pleiotropy)

C-reactive protein levels or triglyceride levels (pleiotropy)

C-reactive protein levels or triglyceride levels (pleiotropy)

Questions about variants on this site