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

Pyridoxine-dependent epilepsy

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

Epilepsy, early-onset, with or without developmental delay

Autosomal dominant epilepsy with auditory features

Autism spectrum disorder - epilepsy - arthrogryposis syndrome

Progressive myoclonic epilepsy type 7

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Familial sleep-related hypermotor epilepsy

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

Focal epilepsy

Pyridoxine-dependent epilepsy

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

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

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Cortical dysplasia-focal epilepsy syndrome

Spinal muscular atrophy-progressive myoclonic epilepsy syndrome

Epilepsy with myoclonic atonic seizures

Epilepsy with myoclonic atonic seizures

Pyridoxine-dependent epilepsy

Progressive myoclonic epilepsy

Questions about variants on this site