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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.

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 · rs1064794053

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs2053619460

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs1596443241

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs1567149943

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs1057520592

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs2053387699

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs767106034

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Sensitive

Intellectual disability-epilepsy-extrapyramidal syndrome

DEAF1 · rs753168686

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Standard

Epilepsy, familial focal, with variable foci 3

NPRL3 · rs2141950212

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs751251777

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs2054212444

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs1064795815

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs2505451976

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs2141755359

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs864309548

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Standard

Epilepsy, familial focal, with variable foci 3

NPRL3 · rs2141981312

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs146691368

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs2505617458

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Standard

Developmental and epileptic encephalopathy 94

CHD2 · rs398122998

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Standard

Epilepsy, familial focal, with variable foci 3

NPRL3 · rs1371859768

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Showing 20 of 20983 · page 13 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.