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.

Glycated hemoglobin levels

Non-small cell lung cancer

Mean corpuscular hemoglobin concentration

Coronary heart disease

Type 2 diabetes

Hematological and biochemical traits

Thyroid volume

Hirschsprung disease

QT interval

Breast cancer

Central corneal thickness

Multiple myeloma

Triglycerides

C-reactive protein

Multiple myeloma

Multiple myeloma

Major depressive disorder in trauma-unexposed individuals

Menopause (age at onset)

Menopause (age at onset)

Platelet count

Questions about variants on this site