249 positions on this site are linked to Hypothyroidism, out of 22,484 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
ITPK1 · rs35332045
See detailed info → Standardnear TMEM121 · rs7143677
See detailed info → Standardnear DPH6 · rs75050808
See detailed info → StandardRASGRP1 · rs55728265
See detailed info → StandardCTCF · rs143016310
See detailed info → StandardZFPM1 · rs4782367
See detailed info → Standardnear NEURL4 · rs3809823
See detailed info → Standardnear CNTROB · rs182554226
See detailed info → Standardnear MAP2K3 · rs12939131
See detailed info → StandardMAPT · rs1529535
See detailed info → Standardnear TBX21 · rs1989291
See detailed info → StandardGALK1 · rs56011703
See detailed info → Standardnear CD7 · rs60894553
See detailed info → Standardnear SS18 · rs2959356
See detailed info → StandardCD226 · rs1790963
See detailed info → StandardIL2RB · rs3218253
See detailed info → StandardSUN2 · rs138716
See detailed info → StandardFAM227B/FGF7 · rs17477923
See detailed info → StandardVEGFA · rs66760320
See detailed info → StandardNEK6 · rs10818937
See detailed info →Showing 20 of 249 · page 12 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.