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 type 9

SCN1A-related epilepsy syndrome, recessive

Familial temporal lobe epilepsy 7

Idiopathic generalized epilepsy

Intellectual disability-epilepsy-extrapyramidal syndrome

Epilepsy, idiopathic generalized, susceptibility to, 13

Epilepsy, idiopathic generalized, susceptibility to, 11

Familial infantile myoclonic epilepsy

Progressive myoclonic epilepsy

Autosomal dominant nocturnal frontal lobe epilepsy 4

Generalized epilepsy-paroxysmal dyskinesia syndrome

Generalized epilepsy-paroxysmal dyskinesia syndrome

Familial temporal lobe epilepsy 7

Epilepsy, childhood absence, susceptibility to, 5

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Progressive myoclonic epilepsy

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

Autosomal dominant nocturnal frontal lobe epilepsy 5

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

Familial focal epilepsy with variable foci

Questions about variants on this site