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

Epilepsy, early-onset, vitamin B6-dependent

Pyridoxine-dependent epilepsy

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

Microcephaly, epilepsy, and diabetes syndrome

Pyridoxine-dependent epilepsy

Pyridoxine-dependent epilepsy

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

Familial sleep-related hypermotor epilepsy

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Progressive myoclonic epilepsy type 3

Inborn genetic diseases

Epilepsy, progressive myoclonic, 3, with intracellular inclusions

Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination

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

Epilepsy, familial focal, with variable foci 2

Epilepsy, early-onset, vitamin B6-dependent

Pyridoxine-dependent epilepsy

Pyridoxine-dependent epilepsy

Progressive myoclonic epilepsy

Questions about variants on this site