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.
SP140 · rs7584894
See detailed info → Sensitivenear HLA-DQB1 · rs28746882
See detailed info → SensitiveIL12A-AS1 · rs570181105
See detailed info → SensitiveGSTM5 · rs368479978
See detailed info → SensitiveSLIT3 · rs150626530
See detailed info → Sensitivenear LRATD1 · rs559664213
See detailed info → Sensitivenear HLA-DQB1 · rs17205731
See detailed info → Sensitivenear CEP162 · rs184104263
See detailed info → SensitiveANKFN1 · rs915504830
See detailed info → SensitiveCCHCR1 · rs886401
See detailed info → SensitiveHISLA · rs17124032
See detailed info → SensitiveRAD17 · rs141495019
See detailed info → Sensitivenear EXTL2 · rs61780263
See detailed info → Sensitivenear HLA-DRB1 · rs2454138
See detailed info → SensitiveLRP2 · rs12988804
See detailed info → SensitivePRDX5 · rs11231749
See detailed info → SensitiveTIMMDC1 · rs9843355
See detailed info → SensitiveSLAMF1 · rs6427540
See detailed info → SensitiveTXK · rs6837324
See detailed info → SensitiveBATF · rs34695601
See detailed info →Showing 20 of 120 · page 1 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.