250 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.
JCAD · rs7920470
See detailed info → StandardEPC1 · rs4291577
See detailed info → StandardCDH23 · rs7101175
See detailed info → Standardnear NKX2-3 · rs10883365
See detailed info → StandardSUFU · rs11191327
See detailed info → StandardAFAP1L2 · rs1931666
See detailed info → Standardnear PLEKHA1 · rs4751889
See detailed info → StandardRNF141 · rs189167758
See detailed info → StandardDKK3 · rs1994842
See detailed info → StandardANO3 · rs34111148
See detailed info → Standardnear EIF3M · rs111632111
See detailed info → StandardPRDM11 · rs7128207
See detailed info → StandardSLC43A3 · rs2729389
See detailed info → StandardCD6 · rs117883663
See detailed info → StandardARAP1 · rs9667947
See detailed info → Standardnear UBAC2 · rs9582285
See detailed info → StandardTGM1 · rs2256989
See detailed info → Standardnear MBIP · rs77916927
See detailed info → StandardRAD51B · rs8008961
See detailed info → Standardnear TMED10 · rs7156476
See detailed info →Showing 20 of 250 · page 11 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.