Gene Knowledge Graph
UTC

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 8, 2026

20,983 positions on this site are linked to Epilepsy, out of 2,507,279 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.

Clear
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

Pyridoxine-dependent epilepsy

ALDH7A1 · rs764417585

See detailed info → Standard

Pyridoxine-dependent epilepsy

ALDH7A1 · rs555896752

See detailed info → Standard

Pyridoxine-dependent epilepsy

ALDH7A1 · rs151107837

See detailed info → Standard

Pyridoxine-dependent epilepsy

ALDH7A1 · rs556400964

See detailed info → Standard

Pyridoxine-dependent epilepsy

ALDH7A1 · rs754449549

See detailed info → Standard

Seizures, benign familial neonatal, 1

KCNQ2 · rs118192226

See detailed info → Standard

Pyridoxine-dependent epilepsy

ALDH7A1 · rs899342601

See detailed info → Sensitive

Cortical dysplasia-focal epilepsy syndrome

CNTNAP2 · rs1085307838

See detailed info → Standard

EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2

GABRG2 · rs121909673

See detailed info → Sensitive

Rett syndrome

MECP2 · rs61748421

See detailed info → Standard

Pyridoxine-dependent epilepsy

ALDH7A1 · rs121912708

See detailed info → Standard

Myoclonic epilepsy of Lafora 2

NHLRC1 · rs28940576

See detailed info → Standard

Idiopathic generalized epilepsy

GABRD · rs2525644185

See detailed info → Standard

Familial infantile myoclonic epilepsy

TBC1D24 · rs748759187

See detailed info → Sensitive

Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome

TBC1D24 · rs564477999

See detailed info → Standard

Episodic ataxia, type 2, and epilepsy

CACNA1A · rs267606696

See detailed info → Sensitive

Spastic paraplegia-severe developmental delay-epilepsy syndrome

HACE1 · rs750371878

See detailed info → Sensitive

Spastic paraplegia-severe developmental delay-epilepsy syndrome

HACE1 · rs759641985

See detailed info → Sensitive

Spastic paraplegia-severe developmental delay-epilepsy syndrome

HACE1 · rs869025280

See detailed info → Standard

Developmental and epileptic encephalopathy

SNAP25 · rs2123120544

See detailed info →

Showing 20 of 20983 · page 11 of 1050

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.