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

Pyridoxine-dependent epilepsy

Pyridoxine-dependent epilepsy

Autosomal dominant epilepsy with auditory features

Polyhydramnios, megalencephaly, and symptomatic epilepsy

Autosomal dominant epilepsy with auditory features

Epilepsy, early-onset, with or without developmental delay

Epilepsy with myoclonic atonic seizures

Pyridoxine-dependent epilepsy

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Epilepsy with myoclonic atonic seizures

Epilepsy, familial focal, with variable foci 2

Epilepsy, X-linked 1, with variable learning disabilities and behavior disorders

Developmental and epileptic encephalopathy

Autosomal dominant nocturnal frontal lobe epilepsy 5

Autosomal dominant nocturnal frontal lobe epilepsy 5

Autosomal dominant nocturnal frontal lobe epilepsy 5

Spinal muscular atrophy-progressive myoclonic epilepsy syndrome

Spinal muscular atrophy-progressive myoclonic epilepsy syndrome

Epilepsy with myoclonic atonic seizures

Cortical dysplasia-focal epilepsy syndrome

Questions about variants on this site