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.

Optic disc size

Serum levels of protein F5

Serum levels of protein SPACA7

SELP protein levels

Cerebrospinal fluid protein SELP levels

SELP protein levels

Adhesion G protein-coupled receptor F5 levels

Serum levels of protein C11orf87

Solute carrier family 22 member 16 levels (SLC22A16.9969.8.3)

Calcium/calmodulin-dependent protein kinase type 1 levels

DNA methylation Hannum age acceleration

Serum levels of protein PLXDC2

SELP protein levels

Protocadherin-9 protein levels (SomaScan ID:3592-4)

Junctophilin-1 levels

Proteasome subunit alpha type-5 levels

Tissue factor pathway inhibitor levels

Solute carrier family 22 member 16 levels

Protein Wnt-3a levels

Tissue factor pathway inhibitor levels

Questions about variants on this site