120 positions on this site are linked to Multiple Sclerosis, out of 108,020 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
CLEC2D · rs7977720
See detailed info → SensitiveSP140 · rs35540610
See detailed info → SensitiveERG · rs6072343
See detailed info → SensitiveTNFAIP8 · rs32658
See detailed info → SensitiveSLC9A8 · rs17785991
See detailed info → SensitiveTHEMIS · rs802730
See detailed info → SensitiveC1orf106 · rs55838263
See detailed info → SensitiveSLC30A7 · rs11581062
See detailed info → SensitiveZNF767 · rs354033
See detailed info → SensitiveMMEL1 · rs4648356
See detailed info → SensitiveIL22RA2 · rs17066096
See detailed info → SensitiveCLECL1 · rs10466829
See detailed info → SensitiveGPR65 · rs2119704
See detailed info → SensitiveCD86 · rs9282641
See detailed info → SensitiveC1orf106 · rs7522462
See detailed info → SensitiveBACH2 · rs12212193
See detailed info → SensitiveAHI1 · rs11154801
See detailed info → SensitiveHLA-DQB1 · rs2040406
See detailed info → SensitiveIRF8 · rs17445836
See detailed info → SensitiveCD58 · rs2300747
See detailed info →Showing 20 of 120 · page 6 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.