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.
SLC14A2 · rs62092159
See detailed info → StandardTNFRSF11A · rs8086340
See detailed info → StandardSBNO2 · rs4807624
See detailed info → StandardPTPRS · rs35324752
See detailed info → StandardTNFSF14 · rs12461880
See detailed info → StandardCERS4 · rs141735698
See detailed info → StandardSMARCA4 · rs117788028
See detailed info → StandardMED26 · rs76065702
See detailed info → Standardnear SLC7A10 · rs34635674
See detailed info → StandardPRX · rs139224539
See detailed info → StandardRELB · rs35194062
See detailed info → Standardnear NTN5 · rs112593985
See detailed info → StandardTMEM86B · rs4374298
See detailed info → StandardZNF460 · rs3746227
See detailed info → Standardnear SNX5 · rs6111715
See detailed info → StandardZMYND8 · rs55994123
See detailed info → StandardPTPN1 · rs6512654
See detailed info → StandardGNAS · rs185799410
See detailed info → Standardnear IFNGR2 · rs969478
See detailed info → Standardnear ZBTB21 · rs28504244
See detailed info →Showing 20 of 249 · page 6 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.