250 positions on this site are linked to Hypothyroidism, out of 22,652 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
near BEND3 · rs12208103
See detailed info → StandardIPCEF1 · rs7770794
See detailed info → Standardnear CARD11 · rs10259879
See detailed info → StandardRAC1 · rs836471
See detailed info → Standardnear CD36 · rs6978235
See detailed info → StandardIRF5 · rs3807307
See detailed info → StandardZC3HAV1 · rs7804956
See detailed info → StandardHIPK2 · rs17262662
See detailed info → Standardnear SARAF · rs79192893
See detailed info → StandardDDHD2 · rs56365338
See detailed info → Standardnear ANKRD46 · rs7825813
See detailed info → Standardnear POU5F1B · rs2124594
See detailed info → Standardnear ADCY8 · rs537496201
See detailed info → StandardTG · rs121912648
See detailed info → StandardTG · rs853316
See detailed info → StandardGLIS3 · rs116915602
See detailed info → Standardnear IFNE · rs4141713
See detailed info → Standardnear SEC61B · rs184293369
See detailed info → Standardnear TMEM236 · rs371858405
See detailed info → Standardnear EBLN1 · rs12766604
See detailed info →Showing 20 of 250 · page 10 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.