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.

PILRB protein levels

X-12063 levels

Serum metabolite levels

CYP3A5 expression (*3 allele)

Methionine sulfone levels

Serum metabolite levels

Ticagrelor levels in individuals with acute coronary syndromes treated with ticagrelor

Condition not named in ClinVar

Condition not named in ClinVar

Condition not named in ClinVar

Condition not named in ClinVar

Condition not named in ClinVar

Condition not named in ClinVar

Condition not named in ClinVar

Condition not named in ClinVar

Condition not named in ClinVar

Condition not named in ClinVar

Condition not named in ClinVar

Condition not named in ClinVar

Condition not named in ClinVar

Questions about variants on this site