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

Cortical dysplasia-focal epilepsy syndrome

Developmental and epileptic encephalopathy

Epilepsy, childhood absence, susceptibility to, 6

Cortical dysplasia-focal epilepsy syndrome

Epilepsy, early-onset, vitamin B6-dependent

Pyridoxine-dependent epilepsy

Progressive myoclonic epilepsy

Generalized epilepsy-paroxysmal dyskinesia syndrome

Familial temporal lobe epilepsy 7

Self-limited epilepsy with centrotemporal spikes

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Pyridoxine-dependent epilepsy

Autosomal dominant nocturnal frontal lobe epilepsy 4

Autosomal dominant nocturnal frontal lobe epilepsy 4

Familial infantile myoclonic epilepsy

Autosomal dominant nocturnal frontal lobe epilepsy 3

Cortical dysplasia-focal epilepsy syndrome

Cortical dysplasia-focal epilepsy syndrome

Severe myoclonic epilepsy in infancy

Autosomal dominant nocturnal frontal lobe epilepsy 4

Questions about variants on this site