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.
TIMMDC1 · rs9843355
See detailed info → SensitiveGFI1 · rs58394161
See detailed info → SensitiveLOC102723854 · rs12478539
See detailed info → SensitiveCD69 · rs11052877
See detailed info → SensitivePRDX5 · rs11231749
See detailed info → SensitiveLTBR · rs12296430
See detailed info → SensitiveCDHR3 · rs73414214
See detailed info → Sensitivenear TTC33 · rs6880778
See detailed info → SensitiveBATF · rs34695601
See detailed info → SensitiveJADE2 · rs2084007
See detailed info → SensitiveBCAS1 · rs2585447
See detailed info → SensitiveDDX6 · rs12365699
See detailed info → SensitiveC1orf106 · rs59655222
See detailed info → SensitiveSMARCA4 · rs12609500
See detailed info → SensitiveIL2RA · rs11256593
See detailed info → SensitiveFCRL3 · rs2317231
See detailed info → SensitiveLOC100506457 · rs11899404
See detailed info → SensitiveIL12A-AS1 · rs1014486
See detailed info → SensitiveLTBR · rs2364485
See detailed info → SensitiveCARD11 · rs1843938
See detailed info →Showing 20 of 120 · page 4 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.