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
9 positions on this site are linked to Epilepsy, out of 2,500,080 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
MECP2 · rs28934904
See detailed info → StandardSCN3A · rs1057518801
See detailed info → StandardSCN1A · rs794726718
See detailed info → StandardSCN1A · rs794726766
See detailed info → StandardSCN1A · rs796053029
See detailed info → StandardSCN1A · rs794726826
See detailed info → StandardSCN1A · rs1057518703
See detailed info → StandardSCN1A · rs796052984
See detailed info → StandardSCN1A · rs121918810
See detailed info →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.