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
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
NPRL3 · rs2141920098
See detailed info → StandardNPRL3 · rs1898688345
See detailed info → StandardCHD2 · rs1567149946
See detailed info → StandardNPRL3 · rs1898844513
See detailed info → StandardCHD2 · rs2141839141
See detailed info → StandardNPRL3 · rs1900184374
See detailed info → StandardCHD2 · rs150951454
See detailed info → SensitiveDEAF1 · rs587777623
See detailed info → StandardCHD2 · rs1064796449
See detailed info → StandardCHD2 · rs2053326002
See detailed info → StandardCHD2 · rs1567138301
See detailed info → SensitiveDEAF1 · rs1064795813
See detailed info → StandardNPRL3 · rs2542813615
See detailed info → StandardCHD2 · rs1131691515
See detailed info → StandardCHD2 · rs2505607968
See detailed info → StandardNPRL3 · rs2542826606
See detailed info → StandardCHD2 · rs397514740
See detailed info → StandardCHD2 · rs758587018
See detailed info → StandardCHD2 · rs864309547
See detailed info → StandardPIGQ · rs778325154
See detailed info →Showing 20 of 20983 · page 14 of 1050
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.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
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.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.