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

Idiopathic generalized epilepsy

Autosomal dominant epilepsy with auditory features

Intellectual disability-epilepsy-extrapyramidal syndrome

Autosomal dominant nocturnal frontal lobe epilepsy 5

Polyhydramnios, megalencephaly, and symptomatic epilepsy

Familial infantile myoclonic epilepsy

Familial temporal lobe epilepsy 7

Epilepsy, familial temporal lobe, 1

Cortical dysplasia-focal epilepsy syndrome

Severe myoclonic epilepsy in infancy

Autosomal dominant nocturnal frontal lobe epilepsy 5

Autosomal dominant nocturnal frontal lobe epilepsy 3

Idiopathic generalized epilepsy

Idiopathic generalized epilepsy

Progressive myoclonic epilepsy type 7

Idiopathic generalized epilepsy

Familial sleep-related hypermotor epilepsy

Autosomal dominant nocturnal frontal lobe epilepsy 5

Epilepsy, idiopathic generalized, susceptibility to, 13

Juvenile myoclonic epilepsy

Questions about variants on this site