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.
TXK · rs6837324
See detailed info → SensitiveLOC101929282 · rs962052
See detailed info → SensitiveFRMD6 · rs11852059
See detailed info → SensitiveNLRC5 · rs8062446
See detailed info → SensitiveTSFM · rs201202118
See detailed info → SensitiveTIMMDC1 · rs1131265
See detailed info → SensitiveBATF · rs34695601
See detailed info → SensitiveIKZF3 · rs9909593
See detailed info → SensitivePRDX5 · rs11231749
See detailed info → SensitivePHGDH · rs483180
See detailed info → SensitiveCD69 · rs11052877
See detailed info → SensitiveLOC102723854 · rs12478539
See detailed info → SensitiveSLC30A7 · rs11578655
See detailed info → SensitiveIL20RA · rs62420820
See detailed info → SensitiveETS1 · rs4262739
See detailed info → SensitiveSLC2A4RG · rs2256814
See detailed info → SensitiveSYDE2 · rs11161550
See detailed info → Sensitivenear TTC33 · rs6880778
See detailed info → SensitiveGFI1 · rs58394161
See detailed info → SensitiveIFNGR2 · rs9808753
See detailed info →Showing 20 of 120 · page 2 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.