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

Neurodevelopmental disorder with epilepsy, spasticity, and brain atrophy

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Microcephaly-intellectual disability-sensorineural hearing loss-epilepsy-abnormal muscle tone syndrome

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Autosomal dominant nocturnal frontal lobe epilepsy 5

Pyridoxine-dependent epilepsy

Pyridoxine-dependent epilepsy

Progressive myoclonic epilepsy type 7

Pyridoxine-dependent epilepsy

Epilepsy, familial temporal lobe, 1

Epilepsy of infancy with migrating focal seizures

Epilepsy with myoclonic atonic seizures

Self-limited epilepsy with centrotemporal spikes

Spinal muscular atrophy-progressive myoclonic epilepsy syndrome

Autism spectrum disorder - epilepsy - arthrogryposis syndrome

Seizure

Epilepsy with myoclonic atonic seizures

Developmental and epileptic encephalopathy, 14

Pyridoxine-dependent epilepsy

Questions about variants on this site