All Variants — MyGeneLog™

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.

Variants linked to Epilepsy

Rett syndrome, zappella variant

Developmental delay

Severe myoclonic epilepsy in infancy

Severe myoclonic epilepsy in infancy

Severe myoclonic epilepsy in infancy

Severe myoclonic epilepsy in infancy

Severe myoclonic epilepsy in infancy

Severe myoclonic epilepsy in infancy

Severe myoclonic epilepsy in infancy

Epilepsy with myoclonic atonic seizures

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Epilepsy, early-onset, vitamin B6-dependent

Infantile epilepsy syndrome

Developmental and epileptic encephalopathy, 4

Epilepsy with myoclonic atonic seizures

Infantile epilepsy syndrome

Developmental and epileptic encephalopathy

Developmental and epileptic encephalopathy

Epilepsy with generalized tonic-clonic seizures

Epilepsy with myoclonic atonic seizures

Questions about variants on this site