23 positions on this site are linked to Benign Nodular Goiter, 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.
PRDM11 · rs3758723
See detailed info → Standardnear IRS1 · rs1316910
See detailed info → Standardnear HES1 · rs4578973
See detailed info → Standardnear OCLN · rs3846487
See detailed info → Standardnear JAZF1 · rs112809701
See detailed info → StandardNRG1 · rs10503921
See detailed info → StandardSULF1 · rs1441197
See detailed info → StandardTG · rs527837819
See detailed info → StandardGLIS3 · rs10974395
See detailed info → StandardMLLT3 · rs1581978
See detailed info → StandardCFAP43 · rs145248574
See detailed info → StandardIMMP1L · rs755188791
See detailed info → StandardITPK1 · rs12101080
See detailed info → StandardSMAD6 · rs12913975
See detailed info → StandardNEB · rs12996964
See detailed info → StandardSGO2 · rs62279324
See detailed info → Standardnear IGFBP5 · rs6754506
See detailed info → StandardKALRN · rs3851352
See detailed info → Standardnear MBIP · rs191713023
See detailed info → StandardDLGAP5 · rs11845848
See detailed info →Showing 20 of 23 · page 1 of 2
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.