249 positions on this site are linked to Hypothyroidism, out of 22,358 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
near ENPP6 · rs6856605
See detailed info → Standardnear EXOC2 · rs762973552
See detailed info → StandardRREB1 · rs7451690
See detailed info → Standardnear PRL · rs6901423
See detailed info → Standardnear SCAND3 · rs186858835
See detailed info → Standardnear GABBR1 · rs115371741
See detailed info → Standardnear HLA-E · rs116894765
See detailed info → Standardnear HLA-DQB2 · rs28893554
See detailed info → StandardDEF6 · rs188443437
See detailed info → StandardC6orf89 · rs79809702
See detailed info → Standardnear TNFAIP3 · rs72980748
See detailed info → StandardHIVEP2 · rs12190804
See detailed info → Standardnear UST · rs7763540
See detailed info → StandardIPCEF1 · rs1406055
See detailed info → Standardnear CEP43 · rs9366078
See detailed info → Standardnear NFE2L3 · rs62446333
See detailed info → StandardCD36 · rs7779119
See detailed info → StandardZC3HAV1 · rs6945954
See detailed info → Standardnear PRAG1 · rs2980769
See detailed info → Standardnear RBPMS · rs62501971
See detailed info →Showing 20 of 249 · page 3 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.