Gene Knowledge Graph
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Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license

Variants linked to Epilepsy

Continuously updated · newest added Nov 11, 2026

20,983 positions on this site are linked to Epilepsy, out of 2,511,480 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

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Recommended (connected, strongest) Strongest evidence Newest Oldest

Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense

← Back to Epilepsy

Standard

Severe myoclonic epilepsy in infancy

SCN1A · rs794726821

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Severe myoclonic epilepsy in infancy

SCN1A · rs794726753

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Severe myoclonic epilepsy in infancy

SCN1A · rs794726761

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Severe myoclonic epilepsy in infancy

SCN1A · rs2468493029

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Severe myoclonic epilepsy in infancy

SCN1A · rs794726790

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Severe myoclonic epilepsy in infancy

SCN1A · rs794726763

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Severe myoclonic epilepsy in infancy

SCN1A · rs794726779

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Severe myoclonic epilepsy in infancy

SCN1A · rs1698960532

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Severe myoclonic epilepsy in infancy

SCN1A · rs796052961

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Severe myoclonic epilepsy in infancy

SCN1A · rs863225035

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Developmental and epileptic encephalopathy

SCN1A · rs1369404945

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Severe myoclonic epilepsy in infancy

SCN1A · rs2468436385

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Severe myoclonic epilepsy in infancy

SCN1A · rs121918753

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Severe myoclonic epilepsy in infancy

SCN1A · rs1553553527

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Severe myoclonic epilepsy in infancy

SCN1A · rs2468182612

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Developmental and epileptic encephalopathy

KCNB1 · rs1984259606

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Severe myoclonic epilepsy in infancy

SCN1A · rs794726839

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Severe myoclonic epilepsy in infancy

SCN1A · rs2105862220

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Severe myoclonic epilepsy in infancy

SCN1A · rs2468220881

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Severe myoclonic epilepsy in infancy

SCN1A · rs1553525325

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Questions about variants on this site

What is a "variant" page on this site?

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.