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.
IRF8 · rs35703946
See detailed info → SensitiveCSF2RB · rs5756405
See detailed info → SensitivePLEK · rs12622670
See detailed info → SensitivePLXNC1 · rs61708525
See detailed info → SensitiveZNF365 · rs61863928
See detailed info → SensitiveEOMES · rs13327021
See detailed info → SensitiveZMIZ1 · rs1250551
See detailed info → SensitiveAGBL2 · rs7120737
See detailed info → SensitiveESPN · rs2986736
See detailed info → SensitiveIL2RA · rs12253981
See detailed info → SensitiveMIR548AN · rs4772201
See detailed info → SensitiveEVI5 · rs11808092
See detailed info → SensitiveC7orf72 · rs10230723
See detailed info → SensitiveWNT9B · rs11871306
See detailed info → SensitiveEVI5 · rs11809700
See detailed info → SensitiveB4GALT5 · rs6020055
See detailed info → SensitiveTXK · rs6837324
See detailed info → SensitiveZC3HAV1 · rs10271373
See detailed info → SensitiveIL20RA · rs62420820
See detailed info → SensitiveSLAMF1 · rs6427540
See detailed info →Showing 20 of 120 · page 3 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.