249 positions on this site are linked to Hypothyroidism, out of 22,526 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
UBASH3A · rs77546520
See detailed info → StandardHORMAD2 · rs6006356
See detailed info → StandardSFI1 · rs1018490
See detailed info → StandardZC3H7B · rs2281333
See detailed info → StandardPER3 · rs12130462
See detailed info → StandardTNFRSF1B · rs235220
See detailed info → StandardCAPZB · rs12091047
See detailed info → StandardGPN2 · rs34204245
See detailed info → StandardMTF1 · rs3891572
See detailed info → StandardSPATA6 · rs77303590
See detailed info → StandardFAF1 · rs17106373
See detailed info → StandardFGGY · rs7516441
See detailed info → StandardVAV3 · rs75778624
See detailed info → Standardnear GSTM4 · rs113581509
See detailed info → StandardDENND2C · rs192422560
See detailed info → Standardnear SLAMF6 · rs151138926
See detailed info → StandardIQSEC1 · rs80136581
See detailed info → StandardTBC1D5 · rs62238493
See detailed info → StandardUBE2E2 · rs11711630
See detailed info → StandardMLH1 · rs3774338
See detailed info →Showing 20 of 249 · page 7 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.