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
ALDH7A1 · rs1064794053
See detailed info → StandardCHD2 · rs2053619460
See detailed info → StandardCHD2 · rs1596443241
See detailed info → StandardCHD2 · rs1567149943
See detailed info → StandardCHD2 · rs1057520592
See detailed info → StandardCHD2 · rs2053387699
See detailed info → StandardCHD2 · rs767106034
See detailed info → SensitiveDEAF1 · rs753168686
See detailed info → StandardNPRL3 · rs2141950212
See detailed info → StandardCHD2 · rs751251777
See detailed info → StandardCHD2 · rs2054212444
See detailed info → StandardCHD2 · rs1064795815
See detailed info → StandardCHD2 · rs2505451976
See detailed info → StandardCHD2 · rs2141755359
See detailed info → StandardCHD2 · rs864309548
See detailed info → StandardNPRL3 · rs2141981312
See detailed info → StandardCHD2 · rs146691368
See detailed info → StandardCHD2 · rs2505617458
See detailed info → StandardCHD2 · rs398122998
See detailed info → StandardNPRL3 · rs1371859768
See detailed info →Showing 20 of 20983 · page 13 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.