249 positions on this site are linked to Hypothyroidism, out of 22,484 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
near EIF3H · rs7822344
See detailed info → Standardnear TNFRSF11B · rs10112995
See detailed info → StandardTG · rs864898
See detailed info → StandardTG · rs2702967
See detailed info → StandardSLC45A4 · rs78622464
See detailed info → StandardZER1 · rs13284665
See detailed info → Standardnear KLF6 · rs10751951
See detailed info → Standardnear PRKCQ · rs11258629
See detailed info → Standardnear FAM107B · rs11812595
See detailed info → Standardnear TMEM236 · rs2436668
See detailed info → StandardJCAD · rs2066332
See detailed info → StandardSGMS1 · rs113171113
See detailed info → StandardVSIR · rs9415996
See detailed info → Standardnear PLEKHA1 · rs4752689
See detailed info → StandardAMPD3 · rs72859115
See detailed info → Standardnear FAM111B · rs185792216
See detailed info → StandardPANX1 · rs11822813
See detailed info → StandardSESN3 · rs2077510
See detailed info → Standardnear FAM76B · rs72981578
See detailed info → StandardCADM1 · rs11605461
See detailed info →Showing 20 of 249 · page 4 of 13
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.