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

Epilepsy, progressive myoclonic, 1B

Epilepsy with myoclonic atonic seizures

Familial sleep-related hypermotor epilepsy

Familial sleep-related hypermotor epilepsy

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

Idiopathic generalized epilepsy

Familial infantile myoclonic epilepsy

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

Generalized epilepsy-paroxysmal dyskinesia syndrome

Pyridoxine-dependent epilepsy

Developmental and epileptic encephalopathy

Idiopathic generalized epilepsy

Generalized epilepsy-paroxysmal dyskinesia syndrome

Epilepsy with myoclonic atonic seizures

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Progressive myoclonic epilepsy type 3

Epilepsy, familial focal, with variable foci 3

Pyridoxine-dependent epilepsy

Epilepsy

Questions about variants on this site