120 positions on this site are linked to Multiple Sclerosis, out of 108,116 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
MIR1204 · rs6990534
See detailed info → SensitiveEPPK1 · rs3923387
See detailed info → SensitiveNCF4 · rs760517
See detailed info → SensitiveZFP36L1 · rs2236262
See detailed info → SensitiveIQCB1 · rs2331964
See detailed info → SensitiveC1orf52 · rs35486093
See detailed info → SensitiveIL2RA · rs12722559
See detailed info → SensitiveATXN1 · rs719316
See detailed info → SensitiveMAF · rs6564681
See detailed info → SensitiveSPRED2 · rs13385171
See detailed info → SensitiveCTSH · rs62013236
See detailed info → SensitiveNR1D1 · rs883871
See detailed info → SensitiveHHEX · rs1112718
See detailed info → SensitiveSAE1 · rs11083862
See detailed info → SensitiveTRIM14 · rs7855251
See detailed info → SensitiveLOC102724874 · rs28703878
See detailed info → SensitivePRNCR1 · rs735542
See detailed info → SensitiveSOX8 · rs405343
See detailed info → SensitiveOS9 · rs701006
See detailed info → SensitiveSTAT3 · rs1026916
See detailed info →Showing 20 of 120 · page 5 of 6
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.