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

Epilepsy, childhood absence, susceptibility to, 5

Epilepsy, childhood absence, susceptibility to, 1

Epilepsy, childhood absence, susceptibility to, 1

Epilepsy, idiopathic generalized, susceptibility to, 12

Epilepsy, childhood absence, susceptibility to, 1

Progressive myoclonic epilepsy

Epilepsy, childhood absence, susceptibility to, 5

Epilepsy, childhood absence, susceptibility to, 1

Developmental and epileptic encephalopathy, 43

Epilepsy, childhood absence, susceptibility to, 1

Epilepsy, childhood absence, susceptibility to, 5

Epilepsy, childhood absence, susceptibility to, 1

Progressive myoclonic epilepsy

Epilepsy, idiopathic generalized, susceptibility to, 12

Epilepsy, childhood absence, susceptibility to, 1

GLUT1 deficiency syndrome 1, autosomal recessive

Progressive myoclonic epilepsy type 6

Epilepsy, childhood absence, susceptibility to, 1

Epilepsy, childhood absence, susceptibility to, 5

Progressive myoclonic epilepsy type 6

Questions about variants on this site