249 positions on this site are linked to Hypothyroidism, out of 22,274 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
PTCSC2 · rs7030280
See detailed info → StandardRASGRP1 · rs7173565
See detailed info → StandardPDE10A · rs1079418
See detailed info → Standardnear C1QTNF12 · rs2297864
See detailed info → StandardMICOS10 · rs10917470
See detailed info → Standardnear IL23R · rs11209031
See detailed info → Standardnear S1PR1 · rs2392239
See detailed info → Standardnear GSTM5 · rs11102009
See detailed info → StandardWNT2B · rs536701209
See detailed info → Standardnear ATP1A1 · rs140211448
See detailed info → StandardEDARADD · rs12117927
See detailed info → StandardTHADA · rs11897732
See detailed info → Standardnear PNPT1 · rs9309268
See detailed info → StandardBAZ2B · rs1963848
See detailed info → Standardnear CTLA4 · rs11571297
See detailed info → StandardBHLHE40 · rs11130215
See detailed info → Standardnear EPM2AIP1 · rs11718237
See detailed info → StandardFOXP1 · rs11919503
See detailed info → StandardILDR1 · rs112433403
See detailed info → StandardLPP · rs73192661
See detailed info →Showing 20 of 249 · page 1 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.