19 positions on this site are linked to Systemic Sclerosis, out of 113,783 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
SLC12A5 · rs9074
See detailed info → SensitiveIFNG-AS1 · rs11177005
See detailed info → SensitiveFLNB · rs7355798
See detailed info → SensitiveTNFAIP3 · rs5029949
See detailed info → SensitiveDDX6 · rs10892286
See detailed info → SensitiveAHNAK2 · rs11851053
See detailed info → SensitiveTNFSF4 · rs10912594
See detailed info → SensitiveTNFSF4 · rs844663
See detailed info → SensitiveHLA-DPB1 · rs2021408
See detailed info → SensitiveTNIP1 · rs3792783
See detailed info → SensitiveIRF5 · rs36073657
See detailed info → SensitiveFLG2 · rs76285340
See detailed info → SensitiveFLNB · rs4076852
See detailed info → SensitiveIRF5 · rs4731532
See detailed info → SensitiveIGHM · rs45471499
See detailed info → SensitiveBLK · rs2736346
See detailed info → SensitiveTNIP1 · rs2233287
See detailed info → SensitiveSTAT4 · rs3821236
See detailed info → SensitiveTNPO · rs10488631
See detailed info →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.