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

Familial temporal lobe epilepsy 7

Idiopathic generalized epilepsy

Epilepsy, idiopathic generalized, susceptibility to, 15

Epilepsy, early-onset, vitamin B6-dependent

Cortical dysplasia-focal epilepsy syndrome

Epilepsy

Cortical dysplasia-focal epilepsy syndrome

Generalized epilepsy-paroxysmal dyskinesia syndrome

Developmental and epileptic encephalopathy

Familial infantile myoclonic epilepsy

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

Autosomal dominant nocturnal frontal lobe epilepsy 4

Epilepsy, familial focal, with variable foci 2

Epilepsy, idiopathic generalized, susceptibility to, 14

Familial temporal lobe epilepsy 7

Familial infantile myoclonic epilepsy

Epilepsy, idiopathic generalized, susceptibility to, 13

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Progressive myoclonic epilepsy

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Questions about variants on this site