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

Epilepsy, familial focal, with variable foci 1

Progressive myoclonic epilepsy type 7

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

Epilepsy

Pyridoxine-dependent epilepsy

Autism spectrum disorder - epilepsy - arthrogryposis syndrome

Epilepsy, familial temporal lobe, 1

Pyridoxine-dependent epilepsy

Neurodevelopmental disorder with or without early-onset generalized epilepsy

Pyridoxine-dependent epilepsy

Epilepsy, familial focal, with variable foci 2

Pyridoxine-dependent epilepsy

Epilepsy with myoclonic atonic seizures

Epilepsy, progressive myoclonic, 1B

Pyridoxine-dependent epilepsy

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Epilepsy with myoclonic atonic seizures

Progressive myoclonic epilepsy type 3

Spinal muscular atrophy-progressive myoclonic epilepsy syndrome

Autosomal dominant epilepsy

Questions about variants on this site