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.

Chronic lymphocytic leukemia

Chronic lymphocytic leukemia

End-stage renal disease in Type 1 diabetics

Body mass index and fasting glucose (pairwise)

Body mass index and fasting glucose (pairwise)

Body mass index and fasting glucose (pairwise)

Body mass index and triglycerides (pairwise)

Body mass index and triglycerides (pairwise)

Body mass index and HDL-C (pairwise)

Body mass index and HDL-C (pairwise)

Body mass index and HDL-C (pairwise)

Body mass index and HDL-C (pairwise)

Waist-to-hip ratio adjusted for BMI x sex x age interaction (4df test)

Airflow obstruction

Serum ceruloplasmin levels

Chronic lymphocytic leukemia

Sunburns

Neuritic plaque

Dementia and core Alzheimer's disease neuropathologic changes

Toenail selenium levels

Questions about variants on this site