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

Progressive myoclonic epilepsy

Pyridoxine-dependent epilepsy

Progressive myoclonic epilepsy

Progressive myoclonic epilepsy

Epilepsy with myoclonic atonic seizures

Autosomal dominant nocturnal frontal lobe epilepsy 3

Progressive myoclonic epilepsy

Myoclonic epilepsy of Lafora 1

Myoclonic epilepsy of Lafora 1

Progressive myoclonic epilepsy

Polyhydramnios, megalencephaly, and symptomatic epilepsy

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

Autism spectrum disorder - epilepsy - arthrogryposis syndrome

Cortical dysplasia-focal epilepsy syndrome

Autism spectrum disorder - epilepsy - arthrogryposis syndrome

Pyridoxine-dependent epilepsy

Spinal muscular atrophy-progressive myoclonic epilepsy syndrome

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

Developmental and epileptic encephalopathy

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

Questions about variants on this site