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.
MLH1 · rs3774338
See detailed info → StandardTIMMDC1 · rs1599796
See detailed info → StandardCD86 · rs10511408
See detailed info → Standardnear ATP1B3 · rs77557302
See detailed info → Standardnear BCL6 · rs114558062
See detailed info → StandardLPP · rs9864529
See detailed info → StandardMB21D2 · rs6786283
See detailed info → StandardWDR53 · rs78303566
See detailed info → StandardSH3BP2 · rs73082304
See detailed info → Standardnear RBPJ · rs35944082
See detailed info → Standardnear TMEM165 · rs482114
See detailed info → StandardAFF1 · rs17030453
See detailed info → Standardnear H2AZ1 · rs72686215
See detailed info → Standardnear TET2 · rs1490586
See detailed info → Standardnear IL21 · rs6840978
See detailed info → StandardANKRD33B · rs1971974
See detailed info → Standardnear ZNF366 · rs62360622
See detailed info → StandardPDE8B · rs553238971
See detailed info → StandardMACIR · rs2561476
See detailed info → StandardITK · rs865332
See detailed info →Showing 20 of 250 · page 8 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.