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.

TFPI protein levels

Calcium/calmodulin-dependent protein kinase type 1 levels (CAMK1.3592.4.3)

Adhesion G protein-coupled receptor F5 level in Chronic kidney disease with hypertension and no diabetes (6409_57)

Optic disc area

Uncharacterized protein KIAA0040 levels

Coagulation Factor V levels

Junctophilin-1 levels

Sialic acid-binding Ig-like lectin 11 levels (SIGLEC11.8913.22.3)

Sulfotransferase family cytosolic 1B member 1 levels

Sulfotransferase family cytosolic 1B member 1 levels

Angioedema in response to angiotensin-converting enzyme inhibitor

Serum levels of protein CDH7

Serum levels of protein SURF1

Venous thromboembolism

Torsin-1A-interacting protein 1 levels

Solute carrier family 22 member 16 levels

Tissue factor pathway inhibitor levels

Coagulation Factor V levels

Stem cell growth factor beta levels

Stem cell factor levels

Questions about variants on this site