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 temporal lobe, 1

Progressive myoclonic epilepsy type 3

Progressive myoclonic epilepsy

Generalized epilepsy-paroxysmal dyskinesia syndrome

Myoclonic epilepsy, progressive, X-linked

Progressive myoclonic epilepsy type 3

Cortical dysplasia-focal epilepsy syndrome

Epilepsy

Autosomal dominant epilepsy with auditory features

Epilepsy, familial focal, with variable foci 3

Autosomal dominant nocturnal frontal lobe epilepsy 5

Epilepsy with myoclonic atonic seizures

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

Progressive myoclonic epilepsy type 7

Intellectual developmental disorder with or without epilepsy or cerebellar ataxia

Epilepsy, familial focal, with variable foci 3

Developmental and epileptic encephalopathy

Idiopathic generalized epilepsy

Epilepsy, familial focal, with variable foci 3

Epilepsy

Questions about variants on this site