Links from this page to related variants, conditions, drugs and topics are not included for automated readers. Those connections are the Gene Knowledge Graph and are licensed as data: https://www.mygenelog.com/license
11,248 positions on this site are linked to Height, out of 2,507,528 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
Strength of the evidence: all 2+ 3+ 4 Connections: all only those linked to a condition, drug or sense
PAPPA2 · rs10753139
See detailed info → StandardGIT1 · rs3110496
See detailed info → StandardZBTB20 · rs9683251
See detailed info → StandardCMIP · rs2925990
See detailed info → StandardRAD51B · rs1980654
See detailed info → StandardCCDC17 · rs2275086
See detailed info → StandardATF1 · rs10783388
See detailed info → StandardBNC2 · rs4961738
See detailed info → StandardFLI1 · rs654723
See detailed info → Standardnear JCAD · rs2795857
See detailed info → Standardnear LINC00485 · rs7966912
See detailed info → StandardPCSK5 · rs966097
See detailed info → Standardnear NPM1P31 · rs2086945
See detailed info → StandardDENND6A · rs9873524
See detailed info → StandardLTBP1 · rs11685108
See detailed info → StandardGLIS1 · rs4927017
See detailed info → Standardnear LINC01365 · rs2389919
See detailed info → StandardINO80C · rs3088182
See detailed info → Standardnear SPATA31C2 · rs4877421
See detailed info → Standardnear IGF1 · rs855203
See detailed info →Showing 20 of 11248 · page 5 of 563
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.