249 positions on this site are linked to Hypothyroidism, out of 22,358 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
CLNK · rs10003123
See detailed info → StandardIL21 · rs45575135
See detailed info → StandardANKRD33B · rs12187420
See detailed info → StandardSLC25A37 · rs60392867
See detailed info → StandardPIK3R5 · rs1005520
See detailed info → Standardnear TBX21 · rs4794063
See detailed info → StandardNFATC1 · rs113864961
See detailed info → Standardnear SNX5 · rs2745803
See detailed info → StandardCDK6 · rs17766836
See detailed info → StandardRNF141 · rs72859188
See detailed info → StandardC12orf76 · rs12309446
See detailed info → StandardSDF4 · rs12089192
See detailed info → Standardnear ELOA · rs11576333
See detailed info → StandardDNAJC8 · rs510379
See detailed info → StandardFAF1 · rs150957494
See detailed info → StandardLSM3 · rs11128684
See detailed info → Standardnear EPM2AIP1 · rs4678920
See detailed info → StandardZNF589 · rs7651161
See detailed info → StandardSLC39A8 · rs62327954
See detailed info → StandardLRBA · rs6819189
See detailed info →Showing 20 of 249 · page 2 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.