Gene Knowledge Graph
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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.

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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

Epilepsy, familial focal, with variable foci 3

NPRL3 · rs1596528731

See detailed info → Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs2141850583

See detailed info → Standard

Epilepsy, familial focal, with variable foci 3

NPRL3 · rs746975723

See detailed info → Standard

Epilepsy, familial focal, with variable foci 3

NPRL3 · rs1064795838

See detailed info → Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs2505452084

See detailed info → Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs398123000

See detailed info → Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs1057518128

See detailed info → Sensitive

Inborn genetic diseases

CHD2 · rs1555442813

See detailed info → Standard

Epilepsy, familial focal, with variable foci 3

NPRL3 · rs1898806744

See detailed info → Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs761127171

See detailed info → Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs1057519228

See detailed info → Standard

Epilepsy, familial focal, with variable foci 3

NPRL3 · rs2141960559

See detailed info → Standard

Epilepsy, familial focal, with variable foci 3

NPRL3 · rs886037961

See detailed info → Standard

Epilepsy, familial focal, with variable foci 3

NPRL3 · rs1199226176

See detailed info → Standard

Epilepsy

PIGQ · rs200661329

See detailed info → Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs773860345

See detailed info → Standard

Severe myoclonic epilepsy in infancy

SNX27 · rs770358039

See detailed info → Standard

Epilepsy, idiopathic generalized, susceptibility to, 15

RORB · rs2118433023

See detailed info → Standard

Epilepsy

DIAPH1 · rs730882242

See detailed info → Standard

Epilepsy, idiopathic generalized, susceptibility to, 15

RORB · rs1563959514

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Showing 20 of 20983 · page 15 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.